A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257682



Internal ID21399457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95431462..95436138hg38UCSC Ensembl
chr2:96097210..96101886hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg384677
hg194677
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730053
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257682
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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