A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971162



Internal ID22746097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27706961..27711060hg38UCSC Ensembl
chrX:27725078..27729177hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516065, nssv17516066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971162
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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