A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002335



Internal ID19091552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173522833..173583247hg38UCSC Ensembl
Innerchr3:173240623..173301037hg19UCSC Ensembl
Innerchr3:174723317..174783731hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3860415
hg1960415
hg1860415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4986n100
Supporting Variantsnssv3613578, nssv3613576, nssv3613577
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)nsv1002335
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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