A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609868



Internal ID6996787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87716543..87719632hg38UCSC Ensembl
Innerchr6:87716544..87719632hg38UCSC Ensembl
Outerchr6:87716543..87719633hg38UCSC Ensembl
chr6:88426261..88429350hg19UCSC Ensembl
Innerchr6:88426262..88429350hg19UCSC Ensembl
Outerchr6:88426261..88429351hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383090
hg193090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12456500, essv12456497, essv12456501, essv12456496, essv12456502, essv12456495, essv12456498, essv12456499
SamplesHG00261, HG00149, NA12760, NA12489, NA20519, HG00155, NA12874, NA12830
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609868
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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