A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609539



Internal ID20982610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1830290..1879348hg38UCSC Ensembl
chr7:1869926..1918984hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3849059
hg1949059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154810
Samples
Known GenesMAD1L1, MIR4655
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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