A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972333



Internal ID19228134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:60869761..60869822hg38UCSC Ensembl
Outerchr2:61096896..61096957hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123330
Supporting Variants
SamplesKWS2
Known GenesFLJ16341
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972333
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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