A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048642



Internal ID18791173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430431..34464686hg38UCSC Ensembl
Innerchr15:34722632..34756887hg19UCSC Ensembl
Innerchr15:32509924..32544179hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3834256
hg1934256
hg1834256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549407
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048642
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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