A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151118



Internal ID20718158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120654101..120655800hg38UCSC Ensembl
chr7:120294155..120295854hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614053
Supporting Variants
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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