A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619693



Internal ID20992764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14021601..14023200hg38UCSC Ensembl
chr7:14061226..14062825hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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