A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969719



Internal ID22744654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64296260..64315013hg38UCSC Ensembl
chrX:63516140..63534893hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3818754
hg1918754
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516553, nssv17516552
Samples
Known GenesMTMR8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969719
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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