A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660470



Internal ID9926575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36182836..36226978hg38UCSC Ensembl
Outerchr17:36182465..36227348hg38UCSC Ensembl
Innerchr17:34510216..34554422hg19UCSC Ensembl
Outerchr17:34509845..34554792hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3844884
hg1944948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv545e199
Supporting Variantsessv5549904, essv6054715, essv5814807, essv5651689, essv6205307, essv6420687, essv6180739, essv6351134, essv5669936, essv6063646, essv6406012, essv6268492, essv6189114, essv6066863, essv5985494, essv6043484, essv6249881, essv6327283, essv5436959, essv6068875, essv5558459, essv6454682, essv5841836, essv5604524, essv6294372, essv6307910, essv6485280, essv6147112, essv6401447, essv5916398
SamplesHG01441, HG01359, HG01389, HG01456, HG01461, HG01140, HG01350, HG01488, HG01354, HG01495, HG01440, HG01550, HG01124, HG01136, HG01384, HG01149, HG01390, HG01383, HG01497, HG01148, HG01253, HG01113, HG01489, HG01342, HG01491, HG01251, HG01378, HG01125, HG01112, HG01437
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660470
Frequency
Sample Size1151
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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