A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039788



Internal ID21949131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57564160..57568023hg38UCSC Ensembl
chr17:55641521..55645384hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383864
hg193864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626490
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039788
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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