A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383467



Internal ID22441337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97434783..97464202hg38UCSC Ensembl
chr13:98087037..98116456hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3829420
hg1929420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940414
Supporting Variants
Samples
Known GenesRAP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383467
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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