A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046030



Internal ID18788561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99831525..99887655hg38UCSC Ensembl
Innerchr10:101591282..101647412hg19UCSC Ensembl
Innerchr10:101581272..101637402hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3856131
hg1956131
hg1856131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517677
Samples
Known GenesABCC2, DNMBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046030
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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