A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021718



Internal ID19110936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160610141..160647531hg38UCSC Ensembl
Innerchr6:161031173..161068563hg19UCSC Ensembl
Innerchr6:160951163..160988553hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3837391
hg1937391
hg1837391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6167n100
Supporting Variantsnssv3654499
Samples
Known GenesLPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021718
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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