A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957404



Internal ID18858838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136863019..136863073hg38UCSC Ensembl
Outerchr3:136581861..136581915hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114425
Supporting Variants
SamplesKWS1
Known GenesNCK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957404
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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