A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608823



Internal ID20981894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53686003..53687028hg38UCSC Ensembl
chr7:53753696..53754721hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158472
Samples
Known GenesFLJ45974
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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