A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256764



Internal ID21397887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115726328..115730947hg38UCSC Ensembl
chrX:114964203..114971800hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384620
hg197598
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730056
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256764
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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