A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007528



Internal ID18750059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40678818..40757329hg38UCSC Ensembl
Innerchr4:40680835..40759346hg19UCSC Ensembl
Innerchr4:40375592..40454103hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3878512
hg1978512
hg1878512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5195n100
Supporting Variantsnssv3625042
Samples
Known GenesNSUN7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007528
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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