A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832728



Internal ID15779998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96263509..96266550hg38UCSC Ensembl
Innerchr14:96729846..96732887hg19UCSC Ensembl
Innerchr14:95799599..95802640hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383042
hg193042
hg183042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565648
Supporting Variants
Samples
Known GenesBDKRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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