A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277767



Internal ID20486985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42685205..42685205hg38UCSC Ensembl
chrX:42544456..42544456hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277767
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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