A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376973



Internal ID22434843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67858836..68215833hg38UCSC Ensembl
chr17:65854952..66211974hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38356998
hg19357023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934145
Supporting Variants
Samples
Known GenesBPTF, C17orf58, KPNA2, LINC00674, LOC440461
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376973
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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