A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608852



Internal ID20981923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34865301..34875400hg38UCSC Ensembl
chr7:34904913..34915012hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153088
Samples
Known GenesNPSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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