A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601836



Internal ID20974907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101855732..101857906hg38UCSC Ensembl
chr7:101499012..101501186hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151229
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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