A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456801



Internal ID22514681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41000693..41008565hg38UCSC Ensembl
chrX:40859946..40867818hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg387873
hg197873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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