A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813937



Internal ID21259275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107770155..107770241hg38UCSC Ensembl
chr7:107410600..107410686hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710614
Samples
Known GenesSLC26A3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813937
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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