A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965237



Internal ID18253785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180884990..180889664hg38UCSC Ensembl
Innerchr3:180602778..180607452hg19UCSC Ensembl
Innerchr3:182085472..182090146hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384675
hg194675
hg184675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2305789, nssv2305790, nssv2305796, nssv2305788, nssv2305787, nssv2305793, nssv2305794, nssv2305791, nssv2305792, nssv2305795
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965237
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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