A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108647



Internal ID22017880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37009865..37009931hg38UCSC Ensembl
chrX:37027938..37028004hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643981
Samples
Known GenesFAM47C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108647
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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