A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602939



Internal ID20976010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5549783..5550756hg38UCSC Ensembl
chr7:5589414..5590387hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38974
hg19974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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