A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963002



Internal ID18251558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9338733..9339365hg38UCSC Ensembl
Innerchr19:9449409..9450041hg19UCSC Ensembl
Innerchr19:9310409..9311041hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38633
hg19633
hg18633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2131917, nssv2131926, nssv2131920, nssv2131921, nssv2131923, nssv2131924, nssv2131919, nssv2131922, nssv2131918, nssv2131925
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF559, ZNF559-ZNF177
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963002
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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