A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009076



Internal ID18751607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:118028335..118348269hg38UCSC Ensembl
Innerchr4:118949490..119269424hg19UCSC Ensembl
Innerchr4:119168938..119488872hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38319935
hg19319935
hg18319935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5372n100
Supporting Variantsnssv3639338
Samples
Known GenesNDST3, PRSS12, SNHG8, SNORA24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009076
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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