A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606217



Internal ID20979288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92563477..92564009hg38UCSC Ensembl
chr7:92192791..92193323hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159991
Samples
Known GenesFAM133B, FAM133DP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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