A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2762812



Internal ID17802614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139582651..139590050hg38UCSC Ensembl
Innerchr6:139903788..139911187hg19UCSC Ensembl
Innerchr6:139945481..139952880hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg387400
hg197400
hg187400
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv970368
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2762812
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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