A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100234



Internal ID15953420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154654344..154657362hg38UCSC Ensembl
Innerchr7:154446054..154449072hg19UCSC Ensembl
Innerchr7:154076987..154080005hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg383019
hg193019
hg183019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609105
Supporting Variants
Samples
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1100234
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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