A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607810



Internal ID20980881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108175216..108175902hg38UCSC Ensembl
chr7:107815661..107816347hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147011
Samples
Known GenesNRCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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