A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637212



Internal ID7024006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90032777..90034175hg38UCSC Ensembl
Innerchr15:90032827..90034125hg38UCSC Ensembl
Outerchr15:90032727..90034225hg38UCSC Ensembl
chr15:90576009..90577407hg19UCSC Ensembl
Innerchr15:90576059..90577357hg19UCSC Ensembl
Outerchr15:90575959..90577457hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381399
hg191399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317252
SamplesNA18997
Known GenesZNF710
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637212
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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