A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617286



Internal ID20990357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12615801..12617100hg38UCSC Ensembl
chr7:12655426..12656725hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152539
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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