A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955253



Internal ID19206436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85693915..85693980hg38UCSC Ensembl
Outerchr16:85727521..85727586hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127523
Supporting Variants
SamplesKWS1
Known GenesMIR7851
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955253
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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