A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159874



Internal ID20726914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91110868..91111254hg38UCSC Ensembl
chr7:90740183..90740569hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615254
Supporting Variants
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00067


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