A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519588



Internal ID18471183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46287904..46370859hg38UCSC Ensembl
Innerchr10:47659140..47742076hg19UCSC Ensembl
Innerchr10:47129146..47212082hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3882956
hg1982937
hg1882937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051404
Supporting Variants
Samples
Known GenesANTXRL, FAM25B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519588
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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