A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602108



Internal ID20975179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71537196..72256908hg38UCSC Ensembl
chr7:71002181..71721893hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38719713
hg19719713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6900n223
Supporting Variantsnssv18222076
Samples
Known GenesCALN1, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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