A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008795



Internal ID19098013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75732546..76994787hg38UCSC Ensembl
Innerchr3:75781697..77043938hg19UCSC Ensembl
Innerchr3:75864387..77126628hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381262242
hg191262242
hg181262242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3733760
Samples
Known GenesMIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008795
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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