A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957761



Internal ID22732872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29476872..29476872hg38UCSC Ensembl
chrX:29494989..29494989hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453340
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957761
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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