A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873060



Internal ID22648003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49082736..49082901hg38UCSC Ensembl
chrX:48940389..48940554hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465244
Samples
Known GenesWDR45
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873060
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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