A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977739



Internal ID18266259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78769757..78788415hg38UCSC Ensembl
Innerchr15:79062099..79080757hg19UCSC Ensembl
Innerchr15:76849154..76867812hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3818659
hg1918659
hg1818659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2032865, nssv2032874, nssv2032872, nssv2032870, nssv2032867, nssv2032868, nssv2032873, nssv2032866, nssv2032869, nssv2032871
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesADAMTS7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977739
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer