A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604946



Internal ID20978017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115283806..115284442hg38UCSC Ensembl
chr7:114923860..114924496hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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