A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737573



Internal ID161239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130377381..130390000hg38UCSC Ensembl
chrX:129511355..129523974hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3812620
hg1912620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138715
Supporting Variants
Samples
Known GenesGPR119
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737573
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125997


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