A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603460



Internal ID20976531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36500335..36505870hg38UCSC Ensembl
chr7:36539943..36545478hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg385536
hg195536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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