A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977950



Internal ID18613155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29309909..29339257hg38UCSC Ensembl
Innerchr16:29321230..29350578hg19UCSC Ensembl
Innerchr16:29228731..29258079hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3829349
hg1929349
hg1829349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2054286, nssv2054282, nssv2054285, nssv2054287, nssv2054284, nssv2054290, nssv2054283, nssv2054281, nssv2054288, nssv2054289
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSNX29P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977950
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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