A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640028



Internal ID21832075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37010054..37010126hg38UCSC Ensembl
chrX:37028127..37028199hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106209
Supporting Variants
Samples
Known GenesFAM47C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640028
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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