A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600585



Internal ID20973656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5079401..5163100hg38UCSC Ensembl
chr7:5119032..5202731hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3883700
hg1983700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157589
Samples
Known GenesZNF890P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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