A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704863



Internal ID19003144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190750879..190838220hg38UCSC Ensembl
Innerchr1:190720009..190807350hg19UCSC Ensembl
Innerchr1:188986632..189073973hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3887342
hg1987342
hg1887342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011043
Supporting Variants
Samples
Known GenesLOC440704
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3704863
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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