A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050263



Internal ID18792794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43801729..43911849hg38UCSC Ensembl
Innerchr15:44093927..44204047hg19UCSC Ensembl
Innerchr15:41881219..41991339hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38110121
hg19110121
hg18110121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552333
Samples
Known GenesFRMD5, HYPK, MFAP1, PIN4P1, SERF2-C15ORF63, WDR76
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050263
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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