A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033769



Internal ID21943112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76965098..76965167hg38UCSC Ensembl
chr17:74961180..74961249hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033769
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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