A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549001



Internal ID18500596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34427582..34563605hg38UCSC Ensembl
Innerchr15:34719783..34855806hg19UCSC Ensembl
Innerchr15:32507075..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38136024
hg19136024
hg18136024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048580
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3549001
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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