A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3612708



Internal ID18910989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173507505..173571878hg38UCSC Ensembl
Innerchr3:173225295..173289668hg19UCSC Ensembl
Innerchr3:174707989..174772362hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3864374
hg1964374
hg1864374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010872
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)nssv3612708
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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