A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257297



Internal ID21398060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52502140..52510356hg38UCSC Ensembl
chrX:52245675..52253813hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg388217
hg198139
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730276
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257297
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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