A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959245



Internal ID19203724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62799679..62799765hg38UCSC Ensembl
Outerchr9:66455503..66455589hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110018
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959245
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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