A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154810



Internal ID20721850
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 StatusS
Merged Variantsnsv6609539
Supporting Variants
Samples
Known GenesMAD1L1, MIR4655
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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