A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967776



Internal ID18256318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99948092..99950890hg38UCSC Ensembl
Innerchr4:100869249..100872047hg19UCSC Ensembl
Innerchr4:101088272..101091070hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2330209, nssv2330215, nssv2330206, nssv2330210, nssv2330207, nssv2330212, nssv2330214, nssv2330211, nssv2330213, nssv2330208
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesH2AFZ, LOC256880
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967776
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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