A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033608



Internal ID19122829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94405853..94477180hg38UCSC Ensembl
Innerchr5:93741558..93812885hg19UCSC Ensembl
Innerchr5:93767314..93838641hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3871328
hg1971328
hg1871328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747341
Samples
Known GenesKIAA0825
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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