A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131180



Internal ID19282616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43807112..43807176hg38UCSC Ensembl
Outerchr15:44099310..44099374hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970952
SamplesKWS1
Known GenesMFAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131180
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer