A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619315



Internal ID20992386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80465285..80465909hg38UCSC Ensembl
chr7:80094601..80095225hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159148
Samples
Known GenesGNAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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