A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347596



Internal ID21005149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177187272..177190510hg38UCSC Ensembl
chr2:178052000..178055238hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg383239
hg193239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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