A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113724



Internal ID18923649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71975303..71975406hg38UCSC Ensembl
Outerchr15:72267644..72267747hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954384, nssv3969793
SamplesKWS1, KWS2
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113724
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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