A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208951



Internal ID22357101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46584556..46585309hg38UCSC Ensembl
chrX:46443991..46444744hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351103
SamplesHG00731
Known GenesCHST7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208951
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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