A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057875



Internal ID15564375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34235853..34238175hg38UCSC Ensembl
Innerchr6:34203630..34205952hg19UCSC Ensembl
Innerchr6:34311608..34313930hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382323
hg192323
hg182323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602866
Supporting Variants
Samples
Known GenesHMGA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057875
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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