A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256632



Internal ID21400282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108285210..108468457hg38UCSC Ensembl
chr1:108827832..109011079hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38183248
hg19183248
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730086
Supporting Variants
SamplesNA19239
Known GenesNBPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256632
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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