A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457192



Internal ID22515073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30699215..30699309hg38UCSC Ensembl
chrX:30717332..30717426hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868910
Supporting Variants
Samples
Known GenesGK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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