A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976538



Internal ID22751473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110176618..110195125hg38UCSC Ensembl
chrX:109419846..109438353hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3818508
hg1918508
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515113
Samples
Known GenesAMMECR1, TMEM164
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976538
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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