A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271635



Internal ID6620335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64603794..64605014hg38UCSC Ensembl
Innerchr15:64603844..64604964hg38UCSC Ensembl
Outerchr15:64603694..64605114hg38UCSC Ensembl
chr15:64895993..64897213hg19UCSC Ensembl
Innerchr15:64896043..64897163hg19UCSC Ensembl
Outerchr15:64895893..64897313hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636737
Supporting Variants
SamplesNA20785
Known GenesZNF609
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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