A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612122



Internal ID20985193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9949105..10078885hg38UCSC Ensembl
chr7:9988732..10118512hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38129781
hg19129781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6576n223
Supporting Variantsnssv18162426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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