A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969325



Internal ID22744260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63288888..63319114hg38UCSC Ensembl
chrX:62508765..62538993hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3830227
hg1930229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969325
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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