A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339608



Internal ID20997161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99148943..99152665hg38UCSC Ensembl
chr2:99765406..99769128hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg383723
hg193723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090510
Samples
Known GenesC2orf15, TSGA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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