A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639174



Internal ID21831221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47584274..47584274hg38UCSC Ensembl
chrX:47443673..47443673hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059692
Supporting Variants
Samples
Known GenesSYN1, TIMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639174
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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