A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973668



Internal ID18262197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39115807..39116810hg38UCSC Ensembl
Innerchr9:65619052..65620055hg19UCSC Ensembl
Innerchr9:65358872..65359875hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381004
hg191004
hg181004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2738647, nssv2738648, nssv2738650, nssv2738644, nssv2738643, nssv2738645, nssv2738646, nssv2738649, nssv2738642, nssv2738651
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973668
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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