A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031992



Internal ID19121214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55500671..55527017hg38UCSC Ensembl
Innerchr6:55365469..55391815hg19UCSC Ensembl
Innerchr6:55473428..55499774hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3826347
hg1926347
hg1826347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657496
Samples
Known GenesHMGCLL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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