A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957060



Internal ID19217833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:169523887..169523976hg38UCSC Ensembl
Outerchr3:169241675..169241764hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109560
Supporting Variants
SamplesKWS1
Known GenesMECOM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957060
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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