A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457962



Internal ID22515843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20094509..20094568hg38UCSC Ensembl
chrX:20112627..20112686hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872106
Supporting Variants
Samples
Known GenesMAP7D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457962
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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