A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964645



Internal ID18899869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:91140649..91140953hg38UCSC Ensembl
Outerchr8:92152877..92153181hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111740
Supporting Variants
SamplesKWS2
Known GenesLRRC69
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964645
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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