A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972342



Internal ID18607558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64501598..65159836hg38UCSC Ensembl
Innerchr9:42842285..42995364hg19UCSC Ensembl
Innerchr9:42832281..42985360hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38658239
hg19153080
hg18153080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2537227, nssv2537218, nssv2537224, nssv2537225, nssv2537220, nssv2537226, nssv2537219, nssv2537221, nssv2537222, nssv2537223
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAQP7P3, LOC286297
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972342
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