A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617670



Internal ID20990741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29651301..29742600hg38UCSC Ensembl
chr7:29690917..29782216hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3891300
hg1991300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6634n223
Supporting Variantsnssv18219685
Samples
Known GenesDPY19L2P3, LOC646762, MIR550A3, ZNRF2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617670
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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