A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640238



Internal ID21832285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44531270..44531355hg38UCSC Ensembl
chrX:44390516..44390601hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107316
Supporting Variants
Samples
Known GenesFUNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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