A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256228



Internal ID21398562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39824188..39856350hg38UCSC Ensembl
chr9:41969206..42001368hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3832163
hg1932163
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730044
Supporting Variants
SamplesHG00514
Known GenesKGFLP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256228
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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