A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994094



Internal ID19204168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25686305..25687229hg38UCSC Ensembl
Outerchr15:25931452..25932376hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142607
Supporting Variants
SamplesKWS1
Known GenesATP10A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994094
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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