A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938262



Internal ID22713641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58324209..58324306hg38UCSC Ensembl
chr17:56401570..56401667hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371966
Samples
Known GenesBZRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938262
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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