A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701507



Internal ID15438159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109473990..109545257hg38UCSC Ensembl
Innerchr4:110395146..110466413hg19UCSC Ensembl
Innerchr4:110614595..110685862hg18UCSC Ensembl
Innerchr4:110752750..110824017hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3871268
hg1971268
hg1871268
hg1771268
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525385
Supporting Variants
Samples
Known GenesSEC24B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701507
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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