A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636644



Internal ID6676751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59550375..59641686hg38UCSC Ensembl
Innerchr15:59550388..59641673hg38UCSC Ensembl
Outerchr15:59550362..59641699hg38UCSC Ensembl
chr15:59842574..59933885hg19UCSC Ensembl
Innerchr15:59842587..59933872hg19UCSC Ensembl
Outerchr15:59842561..59933898hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3891312
hg1991312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261102
SamplesNA20790
Known GenesGCNT3, GTF2A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636644
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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