A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3498912



Internal ID18739867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152316209..152347401hg38UCSC Ensembl
Innerchr1:152288685..152319877hg19UCSC Ensembl
Innerchr1:150555309..150586501hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3831193
hg1931193
hg1831193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998298
Supporting Variants
Samples
Known GenesFLG, FLG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3498912
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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