A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604677



Internal ID20977748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27396177..27397728hg38UCSC Ensembl
chr7:27435796..27437347hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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