A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616809



Internal ID20989880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115637888..115642499hg38UCSC Ensembl
chr7:115277942..115282553hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg384612
hg194612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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