A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583174



Internal ID21531695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106598509..106600357hg38UCSC Ensembl
chr6:107046384..107048232hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156515
SamplesHG00171
Known GenesRTN4IP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583174
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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