A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15291536



Internal ID1180199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73499178..73515259hg38UCSC Ensembl
Innerchr15:73499179..73515258hg38UCSC Ensembl
Outerchr15:73499177..73515260hg38UCSC Ensembl
chr15:73791519..73807600hg19UCSC Ensembl
Innerchr15:73791520..73807599hg19UCSC Ensembl
Outerchr15:73791518..73807601hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3816082
hg1916082
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636888
Supporting Variants
SamplesHG01060
Known GenesC15orf60
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15291536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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