A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151506



Internal ID20718546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157159724..157160583hg38UCSC Ensembl
chr7:156952418..156953277hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38860
hg19860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418448
Supporting Variants
Samples
Known GenesUBE3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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