A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157907



Internal ID21494100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149626535..149628361hg38UCSC Ensembl
chr6:149947671..149949497hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573191
Supporting Variants
SamplesNA19238
Known GenesKATNA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157907
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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