A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715505



Internal ID16009461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61082059..61083822hg38UCSC Ensembl
Innerchr1:61547731..61549494hg19UCSC Ensembl
Innerchr1:61320319..61322082hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381764
hg191764
hg181764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546370
Supporting Variants
Samples
Known GenesNFIA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv715505
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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