A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529904



Internal ID22399295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29540985..29541037hg38UCSC Ensembl
chr7:29580601..29580653hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8449n152
Supporting Variantsnssv14333913, nssv14333914, nssv14333912, nssv14333911
SamplesHG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529904
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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