A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998992



Internal ID19158528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14467112..14521947hg38UCSC Ensembl
Innerchr4:14468736..14523571hg19UCSC Ensembl
Innerchr4:14077834..14132669hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3854836
hg1954836
hg1854836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619840
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)nsv998992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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