A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256883



Internal ID21400208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60024806..60126538hg38UCSC Ensembl
chr17:58102167..58203899hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38101733
hg19101733
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730213
Supporting Variants
SamplesNA19239
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256883
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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