A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601799



Internal ID20974870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40400687..40584267hg38UCSC Ensembl
chr7:40440286..40623866hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38183581
hg19183581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153779
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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