A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257539



Internal ID21399479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50115707..50346873hg38UCSC Ensembl
chr11:50074878..50306044hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38231167
hg19231167
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730168
Supporting Variants
SamplesHG00733
Known GenesLOC441601
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257539
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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