A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735914



Internal ID19034195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130044843..130174126hg38UCSC Ensembl
Innerchr3:129763686..129892969hg19UCSC Ensembl
Innerchr3:131246376..131375659hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38129284
hg19129284
hg18129284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010790
Supporting Variants
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3735914
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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