A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203761



Internal ID22352722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55402587..55402648hg38UCSC Ensembl
chr7:55470280..55470341hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335436
SamplesNA19240
Known GenesLANCL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203761
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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