A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610735



Internal ID20983806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118810803..119081849hg38UCSC Ensembl
chr7:118450857..118721903hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38271047
hg19271047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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