A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434912



Internal ID22492782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147901976..147904017hg38UCSC Ensembl
chrX:146983494..146985535hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg382042
hg192042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434912
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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