A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322965



Internal ID20856080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:692650..884085hg38UCSC Ensembl
chr2:692650..879771hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38191436
hg19187122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088879
Samples
Known GenesLINC01115
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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