A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1256n106



Internal ID22795084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882856..82888920hg38UCSC Ensembl
chr15:83551608..83557672hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386065
hg196065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111515, nsv1111932, nsv1143397
SamplesKWS2, KWS1
Known GenesHOMER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1256n106
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