A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105449



Internal ID22014682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7081193..7214691hg38UCSC Ensembl
chrX:6999234..7132732hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38133499
hg19133499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648562
Samples
Known GenesHDHD1, MIR4767
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105449
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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