A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874729



Internal ID22649682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64946397..64946746hg38UCSC Ensembl
chrX:64166277..64166626hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469572
Samples
Known GenesZC4H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874729
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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