A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945790



Internal ID18592640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16368744..16369521hg38UCSC Ensembl
Innerchr1:16695239..16696016hg19UCSC Ensembl
Innerchr1:16567826..16568603hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38778
hg19778
hg18778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1756232, nssv1756231, nssv1756234, nssv1756238, nssv1756237, nssv1756235, nssv1756229, nssv1756230, nssv1756236, nssv1756233
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSZRD1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945790
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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