A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024335



Internal ID19113552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9898850..9926287hg38UCSC Ensembl
Innerchr5:9898962..9926399hg19UCSC Ensembl
Innerchr5:9951962..9979399hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3827438
hg1927438
hg1827438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638114, nssv3638118, nssv3638117, nssv3638113, nssv3638116, nssv3638115
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024335
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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