A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636736



Internal ID7023530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64556249..64557931hg38UCSC Ensembl
Innerchr15:64556259..64557922hg38UCSC Ensembl
Outerchr15:64556240..64557941hg38UCSC Ensembl
chr15:64848448..64850130hg19UCSC Ensembl
Innerchr15:64848458..64850121hg19UCSC Ensembl
Outerchr15:64848439..64850140hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15271634
SamplesHG03697
Known GenesZNF609
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636736
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer