A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415706



Internal ID22473576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119096338..119096665hg38UCSC Ensembl
chr6:119417503..119417830hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896813
Supporting Variants
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415706
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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