A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000537



Internal ID21909880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134129639..134129694hg38UCSC Ensembl
chr5:133465330..133465385hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551638
Samples
Known GenesTCF7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000537
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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