A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997526



Internal ID19157062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22047014..22067050hg38UCSC Ensembl
Innerchr4:22048637..22068673hg19UCSC Ensembl
Innerchr4:21657735..21677771hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3820037
hg1920037
hg1820037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5155n100
Supporting Variantsnssv3737714, nssv3619913
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)nsv997526
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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