A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977972



Internal ID19232626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:5604363..5604451hg38UCSC Ensembl
Outerchr1:5664423..5664511hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125167
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977972
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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