A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3478069



Internal ID19067892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58820634..58868721hg38UCSC Ensembl
Innerchr1:59286306..59334393hg19UCSC Ensembl
Innerchr1:59058894..59106981hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3848088
hg1948088
hg1848088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014087
Supporting Variants
Samples
Known GenesLINC01135
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3478069
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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