A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009124



Internal ID19098342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62511213..62547620hg38UCSC Ensembl
Innerchr4:63376931..63413338hg19UCSC Ensembl
Innerchr4:63059526..63095933hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3836408
hg1936408
hg1836408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5221n100
Supporting Variantsnssv3739499, nssv3739500
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009124
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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