A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611694



Internal ID20984765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2709045..2712468hg38UCSC Ensembl
chr7:2748679..2752102hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383424
hg193424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157008
Samples
Known GenesAMZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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