A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437876



Internal ID22104057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41167747..41167837hg38UCSC Ensembl
chr17:39323999..39324089hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767928
Samples
Known GenesKRTAP4-3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437876
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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