A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101780



Internal ID22011013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133642490..133642605hg38UCSC Ensembl
chrX:132776518..132776633hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646929
Samples
Known GenesGPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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