A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000544



Internal ID19089761
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 StatusM
Merged Variants
Supporting Variantsnssv3639236
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)nsv1000544
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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