A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256435



Internal ID21400343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95428113..95466225hg38UCSC Ensembl
chr2:96093861..96131973hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3838113
hg1938113
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730053
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256435
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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