A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258656



Internal ID21398814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50132556..50347138hg38UCSC Ensembl
chr11:50091727..50306309hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38214583
hg19214583
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730168
Supporting Variants
SamplesHG00731
Known GenesLOC441601
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258656
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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