A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257448



Internal ID21397952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6044555..6160289hg38UCSC Ensembl
chr21:44797853..44913889hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38115735
hg19116037
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730046
Supporting Variants
SamplesHG00512
Known GenesLINC00313, LINC00319, SIK1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257448
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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