A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615581



Internal ID20988652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86676824..86714502hg38UCSC Ensembl
chr7:86306140..86343818hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3837679
hg1937679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160422
Samples
Known GenesGRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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