A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974787



Internal ID18263310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24998709..24999209hg38UCSC Ensembl
Innerchr16:25010030..25010530hg19UCSC Ensembl
Innerchr16:24917531..24918031hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2052946, nssv2052943, nssv2052940, nssv2052942, nssv2052938, nssv2052944, nssv2052939, nssv2052945, nssv2052947, nssv2052941
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesARHGAP17
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974787
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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