A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970202



Internal ID18899272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93785902..93786215hg38UCSC Ensembl
Outerchr1:94251458..94251771hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133879
Supporting Variants
SamplesKWS2
Known GenesBCAR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970202
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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