A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602120



Internal ID20975191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96855428..96866658hg38UCSC Ensembl
chr7:96484740..96495970hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811231
hg1911231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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