A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438327



Internal ID22496197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147187238..147196547hg38UCSC Ensembl
chrX:146268756..146278065hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg389310
hg199310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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