A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616524



Internal ID20989595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16812757..16854611hg38UCSC Ensembl
chr7:16852381..16894235hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3841855
hg1941855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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