A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044804



Internal ID18787335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34379873..34522329hg38UCSC Ensembl
Innerchr15:34672074..34814530hg19UCSC Ensembl
Innerchr15:32459366..32601822hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38142457
hg19142457
hg18142457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2553n100
Supporting Variantsnssv3721661, nssv3721662
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044804
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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