A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456717



Internal ID22514596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45941648..45943636hg38UCSC Ensembl
chrX:45801083..45803071hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456717
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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