A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998134



Internal ID19157671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35676753..35715858hg38UCSC Ensembl
Innerchr4:35678375..35717480hg19UCSC Ensembl
Innerchr4:35354770..35393875hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3839106
hg1939106
hg1839106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5191n100
Supporting Variantsnssv3625026, nssv3739348
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)nsv998134
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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