A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508043



Internal ID22565992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78693679..78695436hg38UCSC Ensembl
chr6:79403396..79405153hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508043
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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