A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617288



Internal ID20990359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40447731..40504946hg38UCSC Ensembl
chr7:40487330..40544545hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3857216
hg1957216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153790
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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