A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467270



Internal ID22525161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44360177..44361171hg38UCSC Ensembl
chrX:44219423..44220417hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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