A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988857



Internal ID19228825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137878212..137879054hg38UCSC Ensembl
Outerchr9:140772664..140773506hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135299
Supporting Variants
SamplesKWS2
Known GenesCACNA1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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