A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969208



Internal ID22744143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152892904..152936381hg38UCSC Ensembl
chrX:152061448..152104925hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3843478
hg1943478
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515646, nssv17515647
Samples
Known GenesZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969208
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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