A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569179



Internal ID21517534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162125401..162125537hg38UCSC Ensembl
chr5:161552407..161552543hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130806
SamplesNA19238
Known GenesGABRG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569179
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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