A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148551



Internal ID20715592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112265182..112265517hg38UCSC Ensembl
chr7:111905237..111905572hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605471
Supporting Variants
Samples
Known GenesZNF277
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00103


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