A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027007



Internal ID18769539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89099218..89628146hg38UCSC Ensembl
Innerchr6:89808937..90337865hg19UCSC Ensembl
Innerchr6:89865656..90394586hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38528929
hg19528929
hg18528931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648954
Samples
Known GenesANKRD6, GABRR1, GABRR2, PM20D2, RRAGD, SRSF12, UBE2J1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027007
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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