A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006022



Internal ID19095240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:91303083..91365639hg38UCSC Ensembl
Innerchr1:91768640..91831196hg19UCSC Ensembl
Innerchr1:91541228..91603784hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3862557
hg1962557
hg1862557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482036
Samples
Known GenesHFM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006022
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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