A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631781



Internal ID6671906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36305043..36307489hg38UCSC Ensembl
Innerchr13:36305082..36307451hg38UCSC Ensembl
Outerchr13:36305005..36307528hg38UCSC Ensembl
chr13:36879180..36881626hg19UCSC Ensembl
Innerchr13:36879219..36881588hg19UCSC Ensembl
Outerchr13:36879142..36881665hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382447
hg192447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14691662
SamplesHG03868
Known GenesSPG20
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631781
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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