A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968815



Internal ID18892140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:101479244..101479309hg38UCSC Ensembl
Outerchr12:101873022..101873087hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113514
Supporting Variants
SamplesKWS2
Known GenesSPIC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968815
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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