A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421918



Internal ID21079471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141669797..141670109hg38UCSC Ensembl
chr7:141369597..141369909hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150776
Samples
Known GenesKIAA1147
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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