A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997252



Internal ID20564292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124072001..124072800hg38UCSC Ensembl
chr12:124556548..124557347hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485910
Supporting Variants
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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