A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053629



Internal ID21962862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8801228..8801228hg38UCSC Ensembl
chrX:8769269..8769269hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642104
Samples
Known GenesFAM9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053629
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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