A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603996



Internal ID20977067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121918045..121918655hg38UCSC Ensembl
chr7:121558099..121558709hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151827
Samples
Known GenesPTPRZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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