A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057643



Internal ID15910829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33174762..33288694hg38UCSC Ensembl
Innerchr6:33142539..33256471hg19UCSC Ensembl
Innerchr6:33250517..33364449hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38113933
hg19113933
hg18113933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602830
Supporting Variants
Samples
Known GenesB3GALT4, COL11A2, HCG25, HSD17B8, MIR219-1, MIR6873, RING1, RPS18, RXRB, SLC39A7, VPS52, WDR46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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