A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997319



Internal ID19156857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22047890..22069078hg38UCSC Ensembl
Innerchr4:22049513..22070701hg19UCSC Ensembl
Innerchr4:21658611..21679799hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3821189
hg1921189
hg1821189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5155n100
Supporting Variantsnssv3620579, nssv3620577, nssv3620578
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)nsv997319
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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