A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127436



Internal ID18925887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:58620649..58620967hg38UCSC Ensembl
Outerchr15:58912848..58913166hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3955135
SamplesKWS1
Known GenesADAM10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127436
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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