A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736330



Internal ID159996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28473488..28525488hg38UCSC Ensembl
chrX:28491605..28543605hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3852001
hg1952001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138953
Supporting Variants
Samples
Known GenesMIR6134
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736330
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000626959


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