A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609065



Internal ID6649297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55369940..55373258hg38UCSC Ensembl
Innerchr6:55369966..55373232hg38UCSC Ensembl
Outerchr6:55369914..55373284hg38UCSC Ensembl
chr6:55234738..55238056hg19UCSC Ensembl
Innerchr6:55234764..55238030hg19UCSC Ensembl
Outerchr6:55234712..55238082hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg383319
hg193319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12361780
SamplesNA21123
Known GenesGFRAL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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