A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2763139



Internal ID17380841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22671337..22682562hg38UCSC Ensembl
Innerchr7:22710956..22722181hg19UCSC Ensembl
Innerchr7:22677481..22688706hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3811226
hg1911226
hg1811226
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971550
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2763139
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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