A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005703



Internal ID19094920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35669992..35713140hg38UCSC Ensembl
Innerchr4:35671614..35714762hg19UCSC Ensembl
Innerchr4:35348009..35391157hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3843149
hg1943149
hg1843149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5191n100
Supporting Variantsnssv3739344
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)nsv1005703
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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