A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3603694



Internal ID18901975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130039363..130117757hg38UCSC Ensembl
Innerchr3:129758206..129836600hg19UCSC Ensembl
Innerchr3:131240896..131319290hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3878395
hg1978395
hg1878395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004203
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)nssv3603694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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