A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145098



Internal ID18910218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:37169824..37170324hg38UCSC Ensembl
Outerchr6:37137600..37138100hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982179
SamplesKWS1
Known GenesPIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145098
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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