A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144155



Internal ID18910049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:192500..193600hg38UCSC Ensembl
Outerchr7:192500..193600hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994878
SamplesKWS1
Known GenesFAM20C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144155
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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