A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156112



Internal ID20723152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:324612..416918hg38UCSC Ensembl
chr7:364578..456884hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3892307
hg1992307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613738
Supporting Variants
Samples
Known GenesLOC442497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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