A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103903



Internal ID22013136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64938281..64938367hg38UCSC Ensembl
chrX:64158161..64158247hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638538
Samples
Known GenesZC4H2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103903
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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