A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2557377



Internal ID17425202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92139786..92145991hg38UCSC Ensembl
Innerchr9:94902068..94908273hg19UCSC Ensembl
Innerchr9:93941889..93948094hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386206
hg196206
hg186206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972778
Supporting Variants
SamplesHGDP00542
Known GenesLINC00475
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)nssv2557377
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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