A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001845



Internal ID19091062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75546018hg38UCSC Ensembl
Innerchr3:75427095..75595169hg19UCSC Ensembl
Innerchr3:75509785..75677859hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38168075
hg19168075
hg18168075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3602323
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)nsv1001845
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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