A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646688



Internal ID21838735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7844600..8466547hg38UCSC Ensembl
chrX:7812641..8434588hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38621948
hg19621948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102001
Supporting Variants
Samples
Known GenesMIR651, PNPLA4, VCX2, VCX3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646688
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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