A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv176n137



Internal ID22812796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45414957..45415212hg38UCSC Ensembl
chr2:45642096..45642351hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2807502, nsv2807503
Samples
Known GenesSRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv176n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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