A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256726



Internal ID21398243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13225176..13235377hg38UCSC Ensembl
chr1:13330735..13340955hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3810202
hg1910221
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730073
Supporting Variants
SamplesHG00513
Known GenesPRAMEF22, PRAMEF3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256726
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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