A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147829



Internal ID20714869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109897304..110005979hg38UCSC Ensembl
chr7:109537361..109646036hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38108676
hg19108676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604626
Supporting Variants
Samples
Known GenesEIF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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