A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977737



Internal ID18612943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75384020..75387694hg38UCSC Ensembl
Innerchr15:75676361..75680035hg19UCSC Ensembl
Innerchr15:73463414..73467088hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg383675
hg193675
hg183675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031027, nssv2031022, nssv2031023, nssv2031028, nssv2031021, nssv2031024, nssv2031020, nssv2031026, nssv2031019, nssv2031025
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSIN3A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977737
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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