A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059711



Internal ID21968944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56773029..56773029hg38UCSC Ensembl
chrX:56799462..56799462hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640157
Samples
Known GenesLOC550643
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059711
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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