A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151485



Internal ID20718525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156903901..156908800hg38UCSC Ensembl
chr7:156696595..156701494hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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