A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156972



Internal ID20724012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21563960..21564638hg38UCSC Ensembl
chr7:21603578..21604256hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616206
Supporting Variants
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0009


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