A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256567



Internal ID21398165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115726533..115729825hg38UCSC Ensembl
chrX:114965311..114971595hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383293
hg196285
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730056
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256567
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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