A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982036



Internal ID18875085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92978318..92978918hg38UCSC Ensembl
Outerchr9:95740600..95741200hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137663
Supporting Variants
SamplesKWS1
Known GenesFGD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982036
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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