A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429990



Internal ID21087543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149602812..149603539hg38UCSC Ensembl
chr7:149299903..149300630hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154043
Samples
Known GenesZNF767
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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