A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452677



Internal ID22510550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71155478..71155529hg38UCSC Ensembl
chrX:70375328..70375379hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872061
Supporting Variants
Samples
Known GenesNLGN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452677
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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