A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704205



Internal ID18655800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143664793..144572337hg38UCSC Ensembl
Innerchr1:149159433..149521828hg19UCSC Ensembl
Innerchr1:147426057..147788452hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38907545
hg19362396
hg18362396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011058
Supporting Variants
Samples
Known GenesFCGR1C, LOC388692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3704205
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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