A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968617



Internal ID19231557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:12657401..12658101hg38UCSC Ensembl
Outerchr18:12657400..12658100hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133420
Supporting Variants
SamplesKWS2
Known GenesSPIRE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968617
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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