A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619756



Internal ID18571351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11356827..12706554hg38UCSC Ensembl
Innerchr4:11358451..12708178hg19UCSC Ensembl
Innerchr4:10967549..12317276hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381349728
hg191349728
hg181349728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010891
Supporting Variants
Samples
Known GenesHS3ST1, MIR572
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3619756
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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