A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643391



Internal ID21835438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37009825..37009893hg38UCSC Ensembl
chrX:37027898..37027966hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102752
Supporting Variants
Samples
Known GenesFAM47C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643391
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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