A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454357



Internal ID22512233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54752342..54753281hg38UCSC Ensembl
chrX:54778775..54779714hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876880
Supporting Variants
Samples
Known GenesITIH6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454357
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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