A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572198



Internal ID21520584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156666793..156667117hg38UCSC Ensembl
chr6:156987927..156988251hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142909
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572198
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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