A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2536032



Internal ID17853445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60878905..60946635hg38UCSC Ensembl
Innerchr9:41465177..41532907hg19UCSC Ensembl
Innerchr9:41455177..41522907hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867731
hg1967731
hg1867731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972697
Supporting Variants
SamplesHGDP01029
Known GenesSPATA31A5, SPATA31A7
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)nssv2536032
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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