A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967549



Internal ID16261505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85570301..85645837hg38UCSC Ensembl
Innerchr3:85619451..85694987hg19UCSC Ensembl
Innerchr3:85702141..85777677hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3875537
hg1975537
hg1875537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590907
Supporting Variants
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967549
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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