A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707146



Internal ID19005427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57712230..57797870hg38UCSC Ensembl
Innerchr10:59471990..59557630hg19UCSC Ensembl
Innerchr10:59141996..59227636hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3885641
hg1985641
hg1885641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035359
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)nssv3707146
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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