A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616801



Internal ID20989872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119525039..119596181hg38UCSC Ensembl
chr7:119165093..119236235hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3871143
hg1971143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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