A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845971



Internal ID22620906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77083366..77089447hg38UCSC Ensembl
chr6:77793083..77799164hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386082
hg196082
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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