A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725974



Internal ID19024255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40202302..40279632hg38UCSC Ensembl
Innerchr2:40429442..40506772hg19UCSC Ensembl
Innerchr2:40282946..40360276hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3877331
hg1977331
hg1877331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008190
Supporting Variants
Samples
Known GenesSLC8A1, SLC8A1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3725974
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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