A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv738178



Internal ID15685448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234609045..234611066hg38UCSC Ensembl
Innerchr1:234744791..234746812hg19UCSC Ensembl
Innerchr1:232811414..232813435hg18UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382022
hg192022
hg182022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549389
Supporting Variants
Samples
Known GenesIRF2BP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv738178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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