A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009775



Internal ID18752306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15216377..15247000hg38UCSC Ensembl
Innerchr3:15257884..15288507hg19UCSC Ensembl
Innerchr3:15232888..15263511hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3830624
hg1930624
hg1830624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593094
Samples
Known GenesCAPN7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009775
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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