A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156071



Internal ID20723111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31984350..31994843hg38UCSC Ensembl
chr7:32023962..32034455hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3810494
hg1910494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611675
Supporting Variants
Samples
Known GenesPDE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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