A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961982



Internal ID18597228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:94814109..94819341hg38UCSC Ensembl
Innerchr2:95479854..95485086hg19UCSC Ensembl
Innerchr2:94843581..94848813hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg385233
hg195233
hg185233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv49n82
Supporting Variantsnssv2674786, nssv2674792, nssv2674794, nssv2674789, nssv2674788, nssv2674793, nssv2674787, nssv2674790, nssv2674791, nssv2676077
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A8P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961982
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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