A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132132



Internal ID21460280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46377645..46377772hg38UCSC Ensembl
chr4:46379662..46379789hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572864
Supporting Variants
SamplesHG02818
Known GenesGABRA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132132
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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