A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962344



Internal ID18250902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56829907..56830788hg38UCSC Ensembl
Innerchr17:54907268..54908149hg19UCSC Ensembl
Innerchr17:52262267..52263148hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38882
hg19882
hg18882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2102993, nssv2102994, nssv2102991, nssv2102988, nssv2102987, nssv2102989, nssv2102990, nssv2102996, nssv2102995, nssv2102992
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesC17orf67
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962344
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer