A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869075



Internal ID22644011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46533534..46536231hg38UCSC Ensembl
chrX:46392969..46395666hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg382698
hg192698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456538
Samples
Known GenesZNF674
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869075
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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