A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582957



Internal ID18881238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149501038..149544678hg38UCSC Ensembl
Innerchr2:150357552..150401192hg19UCSC Ensembl
Innerchr2:150065798..150109438hg18UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg3843641
hg1943641
hg1843641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006441
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)nssv3582957
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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