A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138723



Internal ID21451836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149169085..149169085hg38UCSC Ensembl
chr5:148548648..148548648hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627164
Supporting Variants
SamplesHG01596
Known GenesABLIM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138723
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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