A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351933



Internal ID22577602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9606707..9606707hg38UCSC Ensembl
chr12:9759303..9759303hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969646
Supporting Variants
Samples
Known GenesKLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351933
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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