A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111932



Internal ID19262878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82882856..82888918hg38UCSC Ensembl
Outerchr15:83551608..83557670hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386063
hg196063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1256n106
Supporting Variantsnssv3989050, nssv3989092
SamplesKWS2, KWS1
Known GenesHOMER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111932
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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