A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945946



Internal ID18592796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:52169929..52182878hg38UCSC Ensembl
Innerchr1:52635601..52648550hg19UCSC Ensembl
Innerchr1:52408189..52421138hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3812950
hg1912950
hg1812950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1768263, nssv1768260, nssv1768259, nssv1768258, nssv1768257, nssv1767639, nssv1768262, nssv1768261, nssv1767638, nssv1768256
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZFYVE9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945946
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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