A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999521



Internal ID20566561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14369193..14373030hg38UCSC Ensembl
chr12:14522127..14525964hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg383838
hg193838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468420
Supporting Variants
Samples
Known GenesATF7IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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