A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131063



Internal ID21494003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88194506..88199956hg38UCSC Ensembl
chr4:89115658..89121108hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569614
Supporting Variants
SamplesNA19238
Known GenesABCG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131063
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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