A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639236



Internal ID18937517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115014588..115396763hg38UCSC Ensembl
Innerchr4:115935744..116317919hg19UCSC Ensembl
Innerchr4:116155193..116537368hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38382176
hg19382176
hg18382176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000544
Supporting Variants
Samples
Known GenesNDST4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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