A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974317



Internal ID18262842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24142834..24145405hg38UCSC Ensembl
Innerchr14:24612043..24614614hg19UCSC Ensembl
Innerchr14:23681883..23684454hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382572
hg192572
hg182572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1979543, nssv1979541, nssv1979542, nssv1979547, nssv1979545, nssv1979546, nssv1979548, nssv1979544, nssv1979549, nssv1979550
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR7703, PSME2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974317
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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