A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117472



Internal ID21462732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57618042..57618042hg38UCSC Ensembl
chr20:56193098..56193098hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668338
Supporting Variants
SamplesHG03009
Known GenesZBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117472
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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