A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138206



Internal ID21418176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172076255..172076255hg38UCSC Ensembl
chr5:171503259..171503259hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642784
Supporting Variants
SamplesHG00731
Known GenesSTK10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138206
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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