A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135792



Internal ID18926785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:2611084..2611200hg38UCSC Ensembl
Outerchr12:2720250..2720366hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989380
SamplesKWS2
Known GenesCACNA1C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135792
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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