A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024404



Internal ID19113621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45028977..45071682hg38UCSC Ensembl
Innerchr6:44996714..45039419hg19UCSC Ensembl
Innerchr6:45104692..45147397hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3842706
hg1942706
hg1842706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5958n100
Supporting Variantsnssv3657437, nssv3745479, nssv3657439, nssv3657438, nssv3657436
Samples
Known GenesSUPT3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024404
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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