A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096599



Internal ID20663639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151109061..151112284hg38UCSC Ensembl
chr3:150826848..150830071hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355762
Supporting Variants
Samples
Known GenesMED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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