A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610075



Internal ID20983146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80402257..80583652hg38UCSC Ensembl
chr7:80031573..80212968hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38181396
hg19181396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159143
Samples
Known GenesGNAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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