A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294910



Internal ID20504128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96338557..96338907hg38UCSC Ensembl
chr12:96732335..96732685hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746615
Supporting Variants
Samples
Known GenesCDK17
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294910
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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