A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979885



Internal ID18615086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141599371..141600476hg38UCSC Ensembl
Innerchr3:141318213..141319318hg19UCSC Ensembl
Innerchr3:142800903..142802008hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381106
hg191106
hg181106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2297621, nssv2297625, nssv2297627, nssv2297623, nssv2297618, nssv2297622, nssv2297620, nssv2297624, nssv2297619, nssv2297626
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRASA2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979885
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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