A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2032971



Internal ID17471394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78802587..78806670hg38UCSC Ensembl
Innerchr15:79094929..79099012hg19UCSC Ensembl
Innerchr15:76881984..76886067hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384084
hg194084
hg184084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977740
Supporting Variants
SamplesHGDP00927
Known GenesADAMTS7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2032971
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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