A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034975



Internal ID18777506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10484627..10546155hg38UCSC Ensembl
Innerchr6:10484860..10546388hg19UCSC Ensembl
Innerchr6:10592846..10654374hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3861529
hg1961529
hg1861529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5918n100
Supporting Variantsnssv3654785
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034975
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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