A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142648



Internal ID18903542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166162740..166162827hg38UCSC Ensembl
Outerchr6:166576228..166576315hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994135
SamplesKWS1
Known GenesT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142648
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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