A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976135



Internal ID19228473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33027692..33027743hg38UCSC Ensembl
Outerchr9:33027690..33027741hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137437
Supporting Variants
SamplesKWS2
Known GenesDNAJA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976135
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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