A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258713



Internal ID21397805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40024104..40038210hg38UCSC Ensembl
chr21:41396031..41410137hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3814107
hg1914107
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730189
Supporting Variants
SamplesHG00512
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258713
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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