A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516026



Internal ID18814307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59597851..59609122hg38UCSC Ensembl
Innerchr10:61357609..61368880hg19UCSC Ensembl
Innerchr10:61027615..61038886hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3811272
hg1911272
hg1811272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049492
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)nssv3516026
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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