A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970720



Internal ID22745655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136247268..136254268hg38UCSC Ensembl
chrX:135329427..135336427hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515466
Samples
Known GenesMAP7D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970720
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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