A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153400



Internal ID20720440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129964764..129968374hg38UCSC Ensembl
chr7:129604604..129608214hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg383611
hg193611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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