A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100990



Internal ID22010223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149528451..149528514hg38UCSC Ensembl
chrX:148609990..148610051hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3864
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642849
Samples
Known GenesLINC00893
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100990
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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