A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255877



Internal ID21400409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61845726..61928869hg38UCSC Ensembl
chr9:44981878..45065021hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3883144
hg1983144
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730187
Supporting Variants
SamplesNA19239
Known GenesFAM27C
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255877
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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