A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347348



Internal ID21004901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7088801..7095600hg38UCSC Ensembl
chr2:7228932..7235731hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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