A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110070



Internal ID19260336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137949096..137949364hg38UCSC Ensembl
Outerchr9:140843548..140843816hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959309
SamplesKWS1
Known GenesCACNA1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110070
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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