A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698824



Internal ID21220673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37437676..37438002hg38UCSC Ensembl
chr7:37477279..37477605hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816567
Supporting Variants
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698824
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.734375


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