A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998889



Internal ID19190659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107976849..107976924hg38UCSC Ensembl
Outerchr7:107617294..107617369hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150103
Supporting Variants
SamplesKWB1
Known GenesLAMB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998889
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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