A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699942



Internal ID21221751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44871105..44871178hg38UCSC Ensembl
chr7:44910704..44910777hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699942
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.603448


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