A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154414



Internal ID20721454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137009841..137010615hg38UCSC Ensembl
chr7:136694588..136695362hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424094
Supporting Variants
Samples
Known GenesCHRM2, LOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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