A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610277



Internal ID20983348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118766192..118766642hg38UCSC Ensembl
chr7:118406246..118406696hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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