A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640120



Internal ID21832167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100711327..101398437hg38UCSC Ensembl
chrX:99966323..100653425hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38687111
hg19687103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101606
Supporting Variants
Samples
Known GenesARL13A, BTK, CENPI, CSTF2, DRP2, GLA, NOX1, RPL36A, RPL36A-HNRNPH2, SYTL4, TAF7L, TIMM8A, TMEM35, TRMT2B, XKRX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640120
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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