A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730213



Internal ID21401024
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256960, nssv16256883, nssv16258097, nssv16256866
SamplesNA19239
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730213
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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