A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045362



Internal ID19134581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43988283..44122245hg38UCSC Ensembl
Innerchr15:44280481..44414443hg19UCSC Ensembl
Innerchr15:42067773..42201735hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38133963
hg19133963
hg18133963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552335
Samples
Known GenesFRMD5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045362
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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