A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000678



Internal ID19089895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174068871..174131885hg38UCSC Ensembl
Innerchr3:173786661..173849675hg19UCSC Ensembl
Innerchr3:175269355..175332369hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3863015
hg1963015
hg1863015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613618
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)nsv1000678
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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