A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604684



Internal ID20977755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83459501..83465600hg38UCSC Ensembl
chr7:83088817..83094916hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161009
Samples
Known GenesSEMA3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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