A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045453



Internal ID18787984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2288795..2335989hg38UCSC Ensembl
Innerchr10:2330989..2378183hg19UCSC Ensembl
Innerchr10:2320989..2368183hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3847195
hg1947195
hg1847195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3489713
Samples
Known GenesLINC00701
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045453
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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