A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337165



Internal ID20994718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196018916..196054238hg38UCSC Ensembl
chr2:196883640..196918962hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3835323
hg1935323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081949
Samples
Known GenesDNAH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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