A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477381



Internal ID21134934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71846332..71851459hg38UCSC Ensembl
chr13:72420464..72425591hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg385128
hg195128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012699
Samples
Known GenesDACH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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