A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258290



Internal ID21400797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62420648..62469510hg38UCSC Ensembl
chr9:46731949..46780811hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3848863
hg1948863
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730187
Supporting Variants
SamplesNA19240
Known GenesKGFLP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258290
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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