A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617109



Internal ID20990180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23091901..23101800hg38UCSC Ensembl
chr7:23131520..23141419hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154891
Samples
Known GenesKLHL7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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