A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037972



Internal ID18780503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92261678..92727531hg38UCSC Ensembl
Innerchr15:92804908..93270761hg19UCSC Ensembl
Innerchr15:90605912..91071765hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38465854
hg19465854
hg18465854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555227
Samples
Known GenesC15orf32, FAM174B, LINC00930, ST8SIA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037972
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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