A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997609



Internal ID20564649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15415543..15416508hg38UCSC Ensembl
chr12:15568477..15569442hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472161
Supporting Variants
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00394


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