A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605306



Internal ID20978377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109766081..109770183hg38UCSC Ensembl
chr7:109406138..109410240hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384103
hg194103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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