A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032580



Internal ID19121802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9901840..9926563hg38UCSC Ensembl
Innerchr5:9901952..9926675hg19UCSC Ensembl
Innerchr5:9954952..9979675hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3824724
hg1924724
hg1824724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638174, nssv3638178, nssv3638173, nssv3748672, nssv3638167, nssv3638166, nssv3638170, nssv3748670, nssv3638175, nssv3638172, nssv3638171, nssv3638169, nssv3638168, nssv3638177, nssv3748671, nssv3638176
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)nsv1032580
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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