A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962337



Internal ID18597581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:49400252..49401261hg38UCSC Ensembl
Innerchr17:47477614..47478623hg19UCSC Ensembl
Innerchr17:44832613..44833622hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381010
hg191010
hg181010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2101168, nssv2101170, nssv2101171, nssv2101167, nssv2101172, nssv2101166, nssv2101169, nssv2101173, nssv2101175, nssv2101174
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)nsv962337
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer