A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761904



Internal ID17822297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78810052..78825978hg38UCSC Ensembl
Innerchr6:79519769..79535695hg19UCSC Ensembl
Innerchr6:79576488..79592414hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3815927
hg1915927
hg1815927
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv970720
Supporting Variants
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761904
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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