A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978846



Internal ID18614049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53316077..53414617hg38UCSC Ensembl
Innerchr19:53819330..53917870hg19UCSC Ensembl
Innerchr19:58511142..58609682hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3898541
hg1998541
hg1898541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2156815, nssv2156810, nssv2156809, nssv2156813, nssv2156814, nssv2156811, nssv2156808, nssv2156812, nssv2156807, nssv2156816
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF525, ZNF765, ZNF845
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978846
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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