A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664444



Internal ID9930549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65084887..65774366hg38UCSC Ensembl
chr7:64545265..65239353hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689480
hg19694089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1213e199
Supporting Variantsessv6159037
SamplesHG01051
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664444
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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