A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602393



Internal ID20975464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80784461..80926570hg38UCSC Ensembl
chr7:80413777..80555886hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38142110
hg19142110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160830
Samples
Known GenesSEMA3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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