A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041064



Internal ID18783595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77205561..77339356hg38UCSC Ensembl
Innerchr15:77497903..77631698hg19UCSC Ensembl
Innerchr15:75284958..75418753hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38133796
hg19133796
hg18133796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554586
Samples
Known GenesLINC00597, PEAK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041064
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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