A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978246



Internal ID22753181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52626642..52639459hg38UCSC Ensembl
chrX:52655692..52668509hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3812818
hg1912818
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516339, nssv17516340
Samples
Known GenesSSX8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978246
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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