A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071635



Internal ID21467301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73701745..73701745hg38UCSC Ensembl
chr10:75461503..75461503hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633418
Supporting Variants
SamplesHG03065
Known GenesBMS1P4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071635
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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