A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972314



Internal ID18607530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37477012..37480375hg38UCSC Ensembl
Innerchr9:37477009..37480372hg19UCSC Ensembl
Innerchr9:37467009..37470372hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383364
hg193364
hg183364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2529156, nssv2529151, nssv2529160, nssv2529154, nssv2529152, nssv2529153, nssv2529157, nssv2529155, nssv2529159, nssv2529158
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972314
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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