A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383051



Internal ID22440921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81119674..81119874hg38UCSC Ensembl
chr17:79093474..79093674hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931690
Supporting Variants
Samples
Known GenesAATK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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