A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3554662



Internal ID18506257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84192647..84402534hg38UCSC Ensembl
Innerchr15:84861399..84957232hg19UCSC Ensembl
Innerchr15:82652403..82748236hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38209888
hg1995834
hg1895834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037229
Supporting Variants
Samples
Known GenesGOLGA6L4, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3554662
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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