A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092297



Internal ID21479962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63833753..63833753hg38UCSC Ensembl
chr15:64125952..64125952hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660370
Supporting Variants
SamplesHG03683
Known GenesHERC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092297
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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