A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256721



Internal ID21400255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95610391..95645471hg38UCSC Ensembl
chr2:96276139..96311219hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3835081
hg1935081
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)nssv16256721
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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