A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972697



Internal ID18607913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60878905..60946635hg38UCSC Ensembl
Innerchr9:41465177..41532907hg19UCSC Ensembl
Innerchr9:41455177..41522907hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867731
hg1967731
hg1867731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2536032, nssv2536026, nssv2536031, nssv2536027, nssv2536030, nssv2536028, nssv2536025, nssv2536029, nssv2536034, nssv2536033
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSPATA31A5, SPATA31A7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972697
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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