A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506036



Internal ID18457631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275066..28290212hg38UCSC Ensembl
Innerchr10:28563995..28579141hg19UCSC Ensembl
Innerchr10:28604001..28619147hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3815147
hg1915147
hg1815147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039546
Supporting Variants
Samples
Known GenesMIR8086, MPP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506036
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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