A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15230080



Internal ID5231896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41244034..41245310hg38UCSC Ensembl
Innerchr15:41244089..41245255hg38UCSC Ensembl
Outerchr15:41243979..41245365hg38UCSC Ensembl
chr15:41536232..41537508hg19UCSC Ensembl
Innerchr15:41536287..41537453hg19UCSC Ensembl
Outerchr15:41536177..41537563hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381277
hg191277
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636239
Supporting Variants
SamplesHG03729
Known GenesCHP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15230080
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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