A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542432



Internal ID21866787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3238138..3238138hg38UCSC Ensembl
chr4:3239865..3239865hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065867
Supporting Variants
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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