A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053904



Internal ID15560404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32096949..32203906hg38UCSC Ensembl
Innerchr6:32064726..32171683hg19UCSC Ensembl
Innerchr6:32172704..32279661hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38106958
hg19106958
hg18106958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602104
Supporting Variants
Samples
Known GenesAGER, AGPAT1, ATF6B, EGFL8, FKBPL, GPSM3, LOC100507547, MIR6721, MIR6833, NOTCH4, PBX2, PPT2, PPT2-EGFL8, PRRT1, RNF5, RNF5P1, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053904
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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