A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv728699



Internal ID16022655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169262975..169270354hg38UCSC Ensembl
Innerchr1:169232213..169239592hg19UCSC Ensembl
Innerchr1:167498837..167506216hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg387380
hg197380
hg187380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548168
Supporting Variants
Samples
Known GenesNME7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv728699
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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