A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974763



Internal ID18263286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15408442..15420478hg38UCSC Ensembl
Innerchr16:15502299..15514335hg19UCSC Ensembl
Innerchr16:15409800..15421836hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3812037
hg1912037
hg1812037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2046008, nssv2046007, nssv2046006, nssv2046011, nssv2046009, nssv2046005, nssv2046004, nssv2046003, nssv2046002, nssv2046010
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesMPV17L
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974763
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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