A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258231



Internal ID21398628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54224972..54319002hg38UCSC Ensembl
chr7:54292665..54386695hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3894031
hg1994031
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730048
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258231
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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