A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373568



Internal ID22599237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67640076..67641707hg38UCSC Ensembl
chr17:65636192..65637823hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381632
hg191632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929714
Supporting Variants
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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