A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978552



Internal ID19239068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10414526..10414622hg38UCSC Ensembl
Outerchr18:10414523..10414619hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115990
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978552
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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