A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616923



Internal ID20989994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30390728..30392087hg38UCSC Ensembl
chr7:30430344..30431703hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381360
hg191360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155697
Samples
Known GenesLOC100506516
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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