A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603591



Internal ID20976662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15924392..15949212hg38UCSC Ensembl
chr7:15964017..15988837hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3824821
hg1924821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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