A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502146



Internal ID18800427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2068216..2106060hg38UCSC Ensembl
Innerchr10:2110410..2148254hg19UCSC Ensembl
Innerchr10:2100410..2138254hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3837845
hg1937845
hg1837845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052886
Supporting Variants
Samples
Known GenesMIR6072
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502146
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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