A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2028288



Internal ID17766385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64629802..64634356hg38UCSC Ensembl
Innerchr15:64922001..64926555hg19UCSC Ensembl
Innerchr15:62709054..62713608hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384555
hg194555
hg184555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976944
Supporting Variants
SamplesHGDP00542
Known GenesZNF609
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)nssv2028288
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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