A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984356



Internal ID18619543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75705389..75709671hg38UCSC Ensembl
Innerchr16:75739287..75743569hg19UCSC Ensembl
Innerchr16:74296788..74301070hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg384283
hg194283
hg184283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2067709, nssv2067712, nssv2067708, nssv2067711, nssv2067706, nssv2067710, nssv2067713, nssv2067707, nssv2067715, nssv2067714
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984356
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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