A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963071



Internal ID18251627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52898467..52977616hg38UCSC Ensembl
Innerchr19:53401720..53480869hg19UCSC Ensembl
Innerchr19:58093532..58172681hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3879150
hg1979150
hg1879150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2156484, nssv2156486, nssv2156482, nssv2156481, nssv2156488, nssv2156485, nssv2156483, nssv2156487, nssv2156479, nssv2156480
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF321P, ZNF702P, ZNF816, ZNF816-ZNF321P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963071
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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