A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706218



Internal ID19004499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105385380..105771818hg38UCSC Ensembl
Innerchr10:107145138..107531576hg19UCSC Ensembl
Innerchr10:107135128..107521566hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38386439
hg19386439
hg18386439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050533
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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