A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945732



Internal ID18592583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:727053..794948hg38UCSC Ensembl
Innerchr1:662433..730328hg19UCSC Ensembl
Innerchr1:652296..720191hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3867896
hg1967896
hg1867896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1751296, nssv1751293, nssv1751294, nssv1751298, nssv1751295, nssv1751291, nssv1751292, nssv1751289, nssv1751297, nssv1751290
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100133331, LOC100288069
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945732
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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