A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609207



Internal ID6996129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61593178..61600026hg38UCSC Ensembl
Innerchr6:61593195..61600010hg38UCSC Ensembl
Outerchr6:61593162..61600043hg38UCSC Ensembl
chr6:62303083..62309931hg19UCSC Ensembl
Innerchr6:62303100..62309915hg19UCSC Ensembl
Outerchr6:62303067..62309948hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg386849
hg196849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12387651
SamplesNA19121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609207
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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