A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960771



Internal ID18596018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2670325..2674350hg38UCSC Ensembl
Innerchr19:2670323..2674348hg19UCSC Ensembl
Innerchr19:2621323..2625348hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384026
hg194026
hg184026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2128783, nssv2128786, nssv2128788, nssv2128787, nssv2128790, nssv2128785, nssv2128782, nssv2128784, nssv2128791, nssv2128789
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGNG7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960771
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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