A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633163



Internal ID7019973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92039353..92082679hg38UCSC Ensembl
Innerchr13:92039363..92082670hg38UCSC Ensembl
Outerchr13:92039344..92082689hg38UCSC Ensembl
chr13:92691606..92734932hg19UCSC Ensembl
Innerchr13:92691616..92734923hg19UCSC Ensembl
Outerchr13:92691597..92734942hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3843327
hg1943327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14853656
SamplesHG01673
Known GenesGPC5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633163
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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