A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602314



Internal ID20975385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77641520..77646781hg38UCSC Ensembl
chr7:77270837..77276098hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg385262
hg195262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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