A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631832



Internal ID7018641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39375724..39377077hg38UCSC Ensembl
Innerchr13:39375725..39377076hg38UCSC Ensembl
Outerchr13:39375723..39377078hg38UCSC Ensembl
chr13:39949861..39951214hg19UCSC Ensembl
Innerchr13:39949862..39951213hg19UCSC Ensembl
Outerchr13:39949860..39951215hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14702940
SamplesNA19092
Known GenesLHFP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631832
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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