A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455037



Internal ID22512914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48524233..48524367hg38UCSC Ensembl
chrX:48382621..48382755hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876853
Supporting Variants
Samples
Known GenesEBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455037
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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