A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144726



Internal ID19278005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:30391697..30398997hg38UCSC Ensembl
Outerchr15:30683900..30691200hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg387301
hg197301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981315
SamplesKWS1
Known GenesCHRFAM7A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144726
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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