A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031235



Internal ID18773768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167272147..167359345hg38UCSC Ensembl
Innerchr6:167685635..167772833hg19UCSC Ensembl
Innerchr6:167605625..167692823hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3887199
hg1987199
hg1887199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6197n100
Supporting Variantsnssv3655434, nssv3655433, nssv3655432
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031235
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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