A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955140



Internal ID19221939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63739687..63739752hg38UCSC Ensembl
Outerchr15:64031886..64031951hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127440
Supporting Variants
SamplesKWS1
Known GenesHERC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955140
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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