A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145151



Internal ID18909830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:82443384..82444084hg38UCSC Ensembl
Outerchr7:82072700..82073400hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982233
SamplesKWS1
Known GenesCACNA2D1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145151
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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