A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737825



Internal ID161491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147259259..147264543hg38UCSC Ensembl
chrX:146340777..146346061hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg385285
hg195285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418076
Supporting Variants
Samples
Known GenesMIR509-1, MIR509-2, MIR509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312305


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