A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457980



Internal ID22515861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92125868..92143866hg38UCSC Ensembl
chrX:91380867..91398865hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3817999
hg1917999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879490
Supporting Variants
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457980
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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