A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011970



Internal ID18754506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35924098..35978005hg38UCSC Ensembl
Innerchr4:35925720..35979627hg19UCSC Ensembl
Innerchr4:35602115..35656022hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853908
hg1953908
hg1853908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739349
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)nsv1011970
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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