A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003970



Internal ID19193675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156264605..156267106hg38UCSC Ensembl
Outerchr7:156057299..156059800hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151409
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003970
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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