A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256578



Internal ID21399735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40024797..40037962hg38UCSC Ensembl
chr21:41396724..41409889hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3813166
hg1913166
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730189
Supporting Variants
SamplesHG00733
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256578
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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