A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973657



Internal ID18608872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62503501..62519679hg38UCSC Ensembl
Innerchr9:46814802..46830980hg19UCSC Ensembl
Innerchr9:46654798..46670976hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816179
hg1916179
hg1816179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv91n82
Supporting Variantsnssv2737666, nssv2737661, nssv2737665, nssv2737657, nssv2737659, nssv2737662, nssv2737660, nssv2737664, nssv2737658, nssv2737663
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973657
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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