A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035512



Internal ID21944855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81004041..81020783hg38UCSC Ensembl
chr17:78977841..78994583hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3816743
hg1916743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035512
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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