A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371966



Internal ID22597635
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 StatusS
Merged Variantsnsv5938262
Supporting Variants
Samples
Known GenesBZRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371966
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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