A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039234



Internal ID21948577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56873853..56875001hg38UCSC Ensembl
chr17:54951214..54952362hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039234
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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