A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518120



Internal ID18816401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19030782..19058141hg38UCSC Ensembl
Innerchr10:19319711..19347070hg19UCSC Ensembl
Innerchr10:19359717..19387076hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3827360
hg1927360
hg1827360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049708
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)nssv3518120
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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