A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3602211



Internal ID18900492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75511978hg38UCSC Ensembl
Innerchr3:75427095..75561129hg19UCSC Ensembl
Innerchr3:75509785..75643819hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38134035
hg19134035
hg18134035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011256
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3602211
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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