A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605707



Internal ID20978778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39554001..39640200hg38UCSC Ensembl
chr7:39593600..39679799hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3886200
hg1986200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6653n223
Supporting Variantsnssv18230173
Samples
Known GenesRALA, YAE1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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