A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14337536



Internal ID22201987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107976854..107976924hg38UCSC Ensembl
chr7:107617299..107617369hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196900
Supporting Variants
SamplesHG00732
Known GenesLAMB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14337536
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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