A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989645



Internal ID19229749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:202138959..202156449hg38UCSC Ensembl
Outerchr2:203003682..203021172hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3817491
hg1917491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121726
Supporting Variants
SamplesKWS2
Known GenesLOC100652824
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989645
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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