A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099020



Internal ID21409414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72554030..72554096hg38UCSC Ensembl
chr17:70550170..70550236hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598911
Supporting Variants
SamplesHG00512
Known GenesLINC00673
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099020
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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