A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114425



Internal ID18913374
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 StatusM
Merged Variants
Supporting Variantsnssv3973467, nssv3957404
SamplesKWS2, KWS1
Known GenesNCK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114425
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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