A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963858



Internal ID18862903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93822816..93825700hg38UCSC Ensembl
Outerchr1:94288372..94291256hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382885
hg192885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129587
Supporting Variants
SamplesKWS1
Known GenesBCAR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963858
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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