A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986952



Internal ID19218022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89283375..89283478hg38UCSC Ensembl
Outerchr9:91898290..91898393hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132213
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986952
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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