A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972312



Internal ID18607528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36299954..36314407hg38UCSC Ensembl
Innerchr9:36299951..36314404hg19UCSC Ensembl
Innerchr9:36289951..36304404hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3814454
hg1914454
hg1814454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528796, nssv2528792, nssv2528800, nssv2528797, nssv2528798, nssv2528793, nssv2528795, nssv2528794, nssv2528791, nssv2528799
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)nsv972312
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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