A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967653



Internal ID19245814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:33349699..33349999hg38UCSC Ensembl
Outerchr1:33815300..33815600hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130953
Supporting Variants
SamplesKWS2
Known GenesPHC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967653
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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