A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137046



Internal ID21482358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138434214..138434504hg38UCSC Ensembl
chr5:137769903..137770193hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581222
Supporting Variants
SamplesHG03732
Known GenesKDM3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137046
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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