A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954991



Internal ID19225567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26266626..26266689hg38UCSC Ensembl
Outerchr18:23846590..23846653hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109138
Supporting Variants
SamplesKWS1
Known GenesTAF4B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954991
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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