A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037844



Internal ID21947187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57969296..57969859hg38UCSC Ensembl
chr17:56046657..56047220hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037844
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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