A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107034



Internal ID22016267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30662818..30662869hg38UCSC Ensembl
chrX:30680935..30680986hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639403
Samples
Known GenesGK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107034
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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