A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955977



Internal ID18867083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:166228571..166228633hg38UCSC Ensembl
Outerchr2:167085081..167085143hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136433
Supporting Variants
SamplesKWS1
Known GenesSCN9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955977
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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