A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3604531



Internal ID18556126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123186907..123237744hg38UCSC Ensembl
Innerchr3:122905754..122956591hg19UCSC Ensembl
Innerchr3:124388444..124439281hg18UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3850838
hg1950838
hg1850838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013747
Supporting Variants
Samples
Known GenesSEC22A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3604531
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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