A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493691



Internal ID19081332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6609465..6622192hg38UCSC Ensembl
Innerchr10:6651427..6664154hg19UCSC Ensembl
Innerchr10:6691433..6704160hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812728
hg1912728
hg1812728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047226
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)nssv3493691
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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