A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085944



Internal ID21479985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31963727..31964608hg38UCSC Ensembl
chr17:30290746..30291627hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600103
Supporting Variants
SamplesHG03683
Known GenesSUZ12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085944
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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