A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969819



Internal ID19226579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4687521..4687580hg38UCSC Ensembl
Outerchr16:4737522..4737581hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113749
Supporting Variants
SamplesKWS2
Known GenesMGRN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969819
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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