A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976944



Internal ID18612150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64629802..64634356hg38UCSC Ensembl
Innerchr15:64922001..64926555hg19UCSC Ensembl
Innerchr15:62709054..62713608hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384555
hg194555
hg184555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028288, nssv2028289, nssv2028285, nssv2028287, nssv2026717, nssv2028282, nssv2028283, nssv2026716, nssv2028284, nssv2028286
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF609
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976944
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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