A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990919



Internal ID19237190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41311822..41312232hg38UCSC Ensembl
Outerchr15:41604020..41604430hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138358
Supporting Variants
SamplesKWS2
Known GenesOIP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990919
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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