A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257319



Internal ID21398131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52879830..52975639hg38UCSC Ensembl
chrX:52908860..53004819hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3895810
hg1995960
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730076
Supporting Variants
SamplesHG00513
Known GenesFAM156A, FAM156B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257319
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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