A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523019



Internal ID15450312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83995830..84388348hg38UCSC Ensembl
Innerchr2:84222954..84615472hg19UCSC Ensembl
Innerchr2:84076465..84468983hg18UCSC Ensembl
Innerchr2:84134612..84527130hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38392519
hg19392519
hg18392519
hg17392519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698696
Samples
Known GenesFUNDC2P2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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