A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256991



Internal ID21397815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52903905..52935831hg38UCSC Ensembl
chrX:52932932..52965040hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3831927
hg1932109
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730076
Supporting Variants
SamplesHG00512
Known GenesFAM156A, FAM156B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256991
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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