A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101665



Internal ID22010899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73943254..73943316hg38UCSC Ensembl
chrX:73163089..73163151hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101665
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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