A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638318



Internal ID21830365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50722662..50722770hg38UCSC Ensembl
chrX:50465662..50465770hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107598
Supporting Variants
Samples
Known GenesSHROOM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638318
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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