A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2676699



Internal ID17785187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:94788791..94797491hg38UCSC Ensembl
Innerchr2:95454536..95463236hg19UCSC Ensembl
Innerchr2:94818263..94826963hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg388701
hg198701
hg188701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv979229
Supporting Variants
SamplesHGDP00665
Known GenesANKRD20A8P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2676699
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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