A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015803



Internal ID19105021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160608696..160647502hg38UCSC Ensembl
Innerchr6:161029728..161068534hg19UCSC Ensembl
Innerchr6:160949718..160988524hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3838807
hg1938807
hg1838807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6167n100
Supporting Variantsnssv3654498
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)nsv1015803
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer