A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945995



Internal ID18246159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:71051428..71054541hg38UCSC Ensembl
Innerchr1:71517111..71520224hg19UCSC Ensembl
Innerchr1:71289699..71292812hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg383114
hg193114
hg183114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1771995, nssv1771996, nssv1771997, nssv1771999, nssv1771992, nssv1772000, nssv1771994, nssv1771993, nssv1771991, nssv1771998
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZRANB2-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945995
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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