A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608390



Internal ID20981461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14738764..14881237hg38UCSC Ensembl
chr7:14778389..14920862hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38142474
hg19142474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153880
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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