A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137173



Internal ID18928538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161263104..161263206hg38UCSC Ensembl
Outerchr6:161684136..161684238hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975457, nssv3957788
SamplesKWS1, KWS2
Known GenesAGPAT4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137173
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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