A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016788



Internal ID19106005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34528225..34561388hg38UCSC Ensembl
Innerchr6:34496002..34529165hg19UCSC Ensembl
Innerchr6:34603980..34637143hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3833164
hg1933164
hg1833164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657349
Samples
Known GenesPACSIN1, SPDEF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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