A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980700



Internal ID18615900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96942227..96943843hg38UCSC Ensembl
Innerchr5:96277931..96279547hg19UCSC Ensembl
Innerchr5:96303687..96305303hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381617
hg191617
hg181617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2368556, nssv2370123, nssv2370122, nssv2368552, nssv2368555, nssv2370124, nssv2370121, nssv2368553, nssv2368554, nssv2370125
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLNPEP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980700
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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