A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046832



Internal ID18789363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30644082..30796262hg38UCSC Ensembl
Innerchr15:30936285..31088465hg19UCSC Ensembl
Innerchr15:28723577..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38152181
hg19152181
hg18152181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2533n100
Supporting Variantsnssv3721585
Samples
Known GenesLOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046832
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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