A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737945



Internal ID20513910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41630732..41630863hg38UCSC Ensembl
chr17:39786984..39787115hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279750
Samples
Known GenesKRT42P
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737945
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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