A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125760



Internal ID21417967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36323570..36323570hg38UCSC Ensembl
chr4:36325192..36325192hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607889
Supporting Variants
SamplesHG00731
Known GenesDTHD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125760
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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