A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419266



Internal ID22477136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134491968..134493102hg38UCSC Ensembl
chr6:134813106..134814240hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887976
Supporting Variants
Samples
Known GenesLINC01010
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419266
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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