A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155692



Internal ID20722732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30325688..30328098hg38UCSC Ensembl
chr7:30365304..30367714hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382411
hg192411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617297
Supporting Variants
Samples
Known GenesZNRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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