A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972724



Internal ID18607940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41626878..41649685hg38UCSC Ensembl
Innerchr9:45709944..45735234hg19UCSC Ensembl
Innerchr9:45599940..45625230hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3822808
hg1925291
hg1825291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2541610, nssv2541608, nssv2541607, nssv2541605, nssv2541606, nssv2541604, nssv2541601, nssv2541603, nssv2541602, nssv2541609
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM27A, FAM27E2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972724
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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