A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633351



Internal ID7020160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100762367..100791188hg38UCSC Ensembl
Innerchr13:100762367..100791188hg38UCSC Ensembl
Outerchr13:100761867..100791688hg38UCSC Ensembl
chr13:101414621..101443442hg19UCSC Ensembl
Innerchr13:101414621..101443442hg19UCSC Ensembl
Outerchr13:101414121..101443942hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3828822
hg1928822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14875970
SamplesHG02494
Known GenesNALCN-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633351
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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