A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648562



Internal ID21840609
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 StatusS
Merged Variantsnsv6105449
Supporting Variants
Samples
Known GenesHDHD1, MIR4767
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648562
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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