A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035155



Internal ID21944498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72554030..72554096hg38UCSC Ensembl
chr17:70550170..70550236hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630726
Samples
Known GenesLINC00673
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035155
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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