A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607677



Internal ID20980748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69584124..69591684hg38UCSC Ensembl
chr7:69049110..69056670hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg387561
hg197561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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