A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973741



Internal ID18608956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65792064..65796123hg38UCSC Ensembl
Innerchr9:70369922..70373981hg19UCSC Ensembl
Innerchr9:69609742..69613801hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg384060
hg194060
hg184060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2756015, nssv2750619, nssv2756621, nssv2747918, nssv2754716, nssv2750859, nssv2748019, nssv2753573, nssv2750267, nssv2756584
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)nsv973741
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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