A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14337360



Internal ID22310694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76265819..76266179hg38UCSC Ensembl
chr7:75895137..75895497hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209731
Supporting Variants
SamplesNA19240
Known GenesSRRM3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14337360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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