A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883785



Internal ID22658767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110305940..110306250hg38UCSC Ensembl
chrX:109549168..109549478hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441064
Samples
Known GenesAMMECR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883785
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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