A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962700



Internal ID18876043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:39909052..39909106hg38UCSC Ensembl
Outerchr6:39876828..39876882hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129267
Supporting Variants
SamplesKWS1
Known GenesMOCS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962700
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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