A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615312



Internal ID20988383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99137325..99141136hg38UCSC Ensembl
chr7:98734948..98738759hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383812
hg193812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161321
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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