A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154400



Internal ID20721440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136902655..136903209hg38UCSC Ensembl
chr7:136587402..136587956hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426065
Supporting Variants
Samples
Known GenesCHRM2, LOC349160, MIR490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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