A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610073



Internal ID6996992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96263693..96269931hg38UCSC Ensembl
Innerchr6:96263699..96269926hg38UCSC Ensembl
Outerchr6:96263688..96269937hg38UCSC Ensembl
chr6:96711569..96717807hg19UCSC Ensembl
Innerchr6:96711575..96717802hg19UCSC Ensembl
Outerchr6:96711564..96717813hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386239
hg196239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12472493, essv12472492
SamplesHG03451, HG03376
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610073
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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