A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009002



Internal ID19098220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75420342..75589578hg38UCSC Ensembl
Innerchr3:75469493..75638729hg19UCSC Ensembl
Innerchr3:75552183..75721419hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38169237
hg19169237
hg18169237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4784n100
Supporting Variantsnssv3733710
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)nsv1009002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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