A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340595



Internal ID20998148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226502401..226694400hg38UCSC Ensembl
chr2:227367117..227559116hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38192000
hg19192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087004
Samples
Known GenesMIR5702
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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