A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989865



Internal ID18894795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:36297337..36297737hg38UCSC Ensembl
Outerchr18:33877300..33877700hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136251
Supporting Variants
SamplesKWS2
Known GenesFHOD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989865
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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