A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963340



Internal ID18598581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:94060731..94061342hg38UCSC Ensembl
Innerchr3:93779575..93780186hg19UCSC Ensembl
Innerchr3:95262265..95262876hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38612
hg19612
hg18612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2288598, nssv2288603, nssv2288596, nssv2288601, nssv2288597, nssv2288602, nssv2288599, nssv2288600, nssv2288595, nssv2288594
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDHFRL1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963340
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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