A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989823



Internal ID19236894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:27804679..27805879hg38UCSC Ensembl
Outerchr16:27816000..27817200hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131111
Supporting Variants
SamplesKWS2
Known GenesGSG1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989823
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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