A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972815



Internal ID18608031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33576350..33601972hg38UCSC Ensembl
Innerchr9:33576348..33601970hg19UCSC Ensembl
Innerchr9:33566348..33591970hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3825623
hg1925623
hg1825623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2723042, nssv2723041, nssv2723043, nssv2723044, nssv2723038, nssv2723039, nssv2723037, nssv2723045, nssv2723046, nssv2723040
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)nsv972815
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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