A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124544



Internal ID21418506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49856625..49856720hg38UCSC Ensembl
chr22:50250273..50250368hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591524
Supporting Variants
SamplesHG00731
Known GenesZBED4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124544
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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