A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257403



Internal ID21398335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39604134..39618995hg38UCSC Ensembl
chr9:41749152..41764013hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814862
hg1914862
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730044
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257403
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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