A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013605



Internal ID19102824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10056435..10100768hg38UCSC Ensembl
Innerchr3:10098119..10142452hg19UCSC Ensembl
Innerchr3:10073119..10117452hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3844334
hg1944334
hg1844334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591931
Samples
Known GenesFANCD2, FANCD2OS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013605
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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