A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977696



Internal ID18266216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32610794..32632860hg38UCSC Ensembl
Innerchr15:32902995..32925061hg19UCSC Ensembl
Innerchr15:30690287..30712353hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3822067
hg1922067
hg1822067
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2018347, nssv2018348, nssv2018351, nssv2018350, nssv2018346, nssv2018349, nssv2018352, nssv2018345, nssv2018344, nssv2018343
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARHGAP11A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977696
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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