A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242985



Internal ID22047595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137031296..137031296hg38UCSC Ensembl
chrX:136113455..136113455hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850149
Samples
Known GenesGPR101
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242985
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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