A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234252



Internal ID20801292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122205745..122217329hg38UCSC Ensembl
chr7:121845799..121857383hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3811585
hg1911585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234252
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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