A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449220



Internal ID22507090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144899066..144956312hg38UCSC Ensembl
chrX:143980586..144037832hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3857247
hg1957247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449220
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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