A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107300



Internal ID22016533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72325228..72325330hg38UCSC Ensembl
chrX:71545078..71545180hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107300
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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