A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121156



Internal ID18911220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72093624..72095817hg38UCSC Ensembl
Outerchr15:72385965..72388158hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382194
hg192194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1238n106
Supporting Variantsnssv3964409, nssv3989047
SamplesKWS1, KWS2
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121156
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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