A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232123



Internal ID20799163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124747012..124889814hg38UCSC Ensembl
chr7:124387066..124529868hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38142803
hg19142803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619441
Supporting Variants
Samples
Known GenesGPR37, LOC154872, POT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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