A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852185



Internal ID22627120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6816727..6824308hg38UCSC Ensembl
chr10:6858689..6866270hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387582
hg197582
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452341
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852185
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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