A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100401



Internal ID21429235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8746874..8746874hg38UCSC Ensembl
chr17:8650192..8650192hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661052
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100401
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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