A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974914



Internal ID18871361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123204..69128438hg38UCSC Ensembl
Outerchr9:71738120..71743354hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385235
hg195235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135735
Supporting Variants
SamplesKWS1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974914
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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