A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154623



Internal ID20721663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44805677..44813340hg38UCSC Ensembl
chr7:44845276..44852939hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg387664
hg197664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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