A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997188



Internal ID18848207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:151667074..151667170hg38UCSC Ensembl
Outerchr6:151988209..151988305hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145822
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997188
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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