A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706186



Internal ID19004467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87420044..87502825hg38UCSC Ensembl
Innerchr10:89179801..89262582hg19UCSC Ensembl
Innerchr10:89169781..89252562hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3882782
hg1982782
hg1882782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042899
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)nssv3706186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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