A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256722



Internal ID21400640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:148278093..148342138hg38UCSC Ensembl
chr1:147750211..147814266hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3864046
hg1964056
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730271
Supporting Variants
SamplesNA19240
Known GenesMIR5087, NBPF8
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256722
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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