A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698696



Internal ID15435348
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523019
Supporting Variants
Samples
Known GenesFUNDC2P2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer