A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619283



Internal ID20992354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2789136..2789407hg38UCSC Ensembl
chr7:2828770..2829041hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157052
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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