A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456571



Internal ID22514449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3894368..3902021hg38UCSC Ensembl
chr12:4003534..4011187hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg387654
hg197654
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456571
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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