A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008761



Internal ID19097979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14886395..14950030hg38UCSC Ensembl
Innerchr1:15212891..15276526hg19UCSC Ensembl
Innerchr1:15085478..15149113hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3863636
hg1963636
hg1863636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482225
Samples
Known GenesKAZN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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