A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876895



Internal ID22651857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15957768..15958960hg38UCSC Ensembl
chrX:15975891..15977083hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876895
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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