A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610748



Internal ID20983819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92143301..92143900hg38UCSC Ensembl
chr7:91772615..91773214hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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