A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844102



Internal ID22619037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142061293..142096249hg38UCSC Ensembl
chr6:142382430..142417386hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3834957
hg1934957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501824
Samples
Known GenesNMBR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844102
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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