A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256780



Internal ID21399214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115725492..115729675hg38UCSC Ensembl
chrX:114965461..114972110hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384184
hg196650
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730056
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256780
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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