A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3487439



Internal ID19075080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196772225..196801995hg38UCSC Ensembl
Innerchr1:196741355..196771125hg19UCSC Ensembl
Innerchr1:195007978..195037748hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3829771
hg1929771
hg1829771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009650
Supporting Variants
Samples
Known GenesCFHR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3487439
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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