A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868795



Internal ID22643730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47392961..47396741hg38UCSC Ensembl
chrX:47252360..47256140hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383781
hg193781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467935
Samples
Known GenesZNF157
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868795
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer