A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963001



Internal ID18251557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9214190..9214820hg38UCSC Ensembl
Innerchr19:9324866..9325496hg19UCSC Ensembl
Innerchr19:9185866..9186496hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38631
hg19631
hg18631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2131005, nssv2131009, nssv2131002, nssv2131007, nssv2131004, nssv2131008, nssv2131003, nssv2131010, nssv2131001, nssv2131006
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7D4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963001
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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