A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955122



Internal ID19209860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:39724543..39724596hg38UCSC Ensembl
Outerchr15:40016744..40016797hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127427
Supporting Variants
SamplesKWS1
Known GenesFSIP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955122
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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