A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607288



Internal ID20980359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14705849..14748870hg38UCSC Ensembl
chr7:14745474..14788495hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3843022
hg1943022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153267
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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