A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003504



Internal ID19092722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173883091..174247789hg38UCSC Ensembl
Innerchr3:173600881..173965579hg19UCSC Ensembl
Innerchr3:175083575..175448273hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38364699
hg19364699
hg18364699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613615, nssv3613614, nssv3738377
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)nsv1003504
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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