A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255997



Internal ID21398479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13068691..13122466hg38UCSC Ensembl
chr1:13142562..13189939hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3853776
hg1947378
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730073
Supporting Variants
SamplesHG00514
Known GenesHNRNPCP5
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255997
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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