A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041506



Internal ID18784037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82203823..82289086hg38UCSC Ensembl
Innerchr15:82496164..82581427hg19UCSC Ensembl
Innerchr15:80283219..80368482hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3885264
hg1985264
hg1885264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554618
Samples
Known GenesEFTUD1, FAM154B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041506
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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