A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975968



Internal ID22750903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3814155..3822064hg38UCSC Ensembl
chrX:3732196..3740105hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg387910
hg197910
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2269n209
Supporting Variantsnssv17516208, nssv17516209
Samples
Known GenesLOC389906
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975968
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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