A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961785



Internal ID18597031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:65665921..65670565hg38UCSC Ensembl
Innerchr2:65893055..65897699hg19UCSC Ensembl
Innerchr2:65746559..65751203hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384645
hg194645
hg184645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2175266, nssv2175265, nssv2175261, nssv2175269, nssv2175262, nssv2175264, nssv2175268, nssv2175260, nssv2175267, nssv2175263
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)nsv961785
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