A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3613579



Internal ID18911860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173522833..173585513hg38UCSC Ensembl
Innerchr3:173240623..173303303hg19UCSC Ensembl
Innerchr3:174723317..174785997hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3862681
hg1962681
hg1862681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008730
Supporting Variants
Samples
Known GenesNLGN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3613579
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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