A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945698



Internal ID18592549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10001..22118hg38UCSC Ensembl
Innerchr1:10001..22118hg19UCSC Ensembl
Innerchr1:1..11981hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3812118
hg1912118
hg1811981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n82
Supporting Variantsnssv2576553, nssv2570918, nssv2574189, nssv2570919, nssv2576575, nssv2572825, nssv2576564, nssv2575216, nssv2575439, nssv2571098
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDDX11L1, LOC100288778, MIR6859-1, MIR6859-2, WASH7P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945698
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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