A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596145



Internal ID18894426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75420342..75590743hg38UCSC Ensembl
Innerchr3:75469493..75639894hg19UCSC Ensembl
Innerchr3:75552183..75722584hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38170402
hg19170402
hg18170402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998176
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)nssv3596145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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