A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002031



Internal ID19188211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:869615..869689hg38UCSC Ensembl
Outerchr4:863403..863477hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151095
Supporting Variants
SamplesKWB1
Known GenesGAK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002031
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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