A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340066



Internal ID20997619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177516401..177517900hg38UCSC Ensembl
chr2:178381129..178382628hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082133
Samples
Known GenesAGPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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