A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963011



Internal ID18251567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14799221..14805194hg38UCSC Ensembl
Innerchr19:14910033..14916006hg19UCSC Ensembl
Innerchr19:14771033..14777006hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385974
hg195974
hg185974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2134941, nssv2134940, nssv2134947, nssv2134945, nssv2134948, nssv2134943, nssv2134942, nssv2134939, nssv2134944, nssv2134946
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7C1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963011
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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