A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764154



Internal ID17831404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:77845159..77860051hg38UCSC Ensembl
Innerchr1:78310844..78325736hg19UCSC Ensembl
Innerchr1:78083432..78098324hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3814893
hg1914893
hg1814893
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947433
Supporting Variants
SamplesHGDP00998
Known GenesFAM73A
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764154
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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