A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970600



Internal ID22745535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6906934..7234194hg38UCSC Ensembl
chrX:6824975..7152235hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38327261
hg19327261
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516666
Samples
Known GenesHDHD1, MIR4767, STS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970600
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