A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026260



Internal ID21935603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30969727..30969781hg38UCSC Ensembl
chr17:29296745..29296799hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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