A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609865



Internal ID6996784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87429250..87433611hg38UCSC Ensembl
Innerchr6:87429250..87433611hg38UCSC Ensembl
Outerchr6:87428889..87433824hg38UCSC Ensembl
chr6:88138968..88143329hg19UCSC Ensembl
Innerchr6:88138968..88143329hg19UCSC Ensembl
Outerchr6:88138607..88143542hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384362
hg194362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1200e214
Supporting Variantsessv12456488, essv12456485, essv12456487, essv12456486
SamplesNA20342, NA18879, HG02938, HG03439
Known GenesC6orf165
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609865
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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