A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3554642



Internal ID18506237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84153209..84540375hg38UCSC Ensembl
Innerchr15:84821961..85083606hg19UCSC Ensembl
Innerchr15:82612965..82884610hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38387167
hg19261646
hg18271646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036436
Supporting Variants
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3554642
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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