A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972698



Internal ID18607914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60878905..60890549hg38UCSC Ensembl
Innerchr9:41465177..41476821hg19UCSC Ensembl
Innerchr9:41455177..41466821hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3811645
hg1911645
hg1811645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727308, nssv2727307, nssv2727302, nssv2727303, nssv2727305, nssv2727299, nssv2727306, nssv2727301, nssv2727300, nssv2727304
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972698
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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