A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576922



Internal ID18875203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4663889..4684131hg38UCSC Ensembl
Innerchr2:4711479..4731721hg19UCSC Ensembl
Innerchr2:4689354..4709596hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3820243
hg1920243
hg1820243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003943
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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