A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457201



Internal ID22515082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51038040..51043639hg38UCSC Ensembl
chr12:51431823..51437422hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457201
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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