A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000774



Internal ID18839931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150933060..150933132hg38UCSC Ensembl
Outerchr1:150905536..150905608hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149473
Supporting Variants
SamplesKWB1
Known GenesSETDB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000774
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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