A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095963



Internal ID21430744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50350142..50350525hg38UCSC Ensembl
chr17:48427503..48427886hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586375
Supporting Variants
SamplesHG00731
Known GenesXYLT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095963
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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