A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960789



Internal ID18249350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11725201..11725701hg38UCSC Ensembl
Innerchr19:11836016..11836516hg19UCSC Ensembl
Innerchr19:11697016..11697516hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2132556, nssv2132562, nssv2132560, nssv2132563, nssv2132558, nssv2132559, nssv2132557, nssv2132561, nssv2132555, nssv2132564
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF823
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960789
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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