A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984258



Internal ID18619446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11926165..11927805hg38UCSC Ensembl
Innerchr16:12020022..12021662hg19UCSC Ensembl
Innerchr16:11927523..11929163hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381641
hg191641
hg181641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2628021, nssv2628025, nssv2628024, nssv2628028, nssv2628022, nssv2628026, nssv2628027, nssv2628023, nssv2628019, nssv2628020
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984258
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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