A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091992



Internal ID15598492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102385213..102473462hg38UCSC Ensembl
Innerchr7:102025660..102113909hg19UCSC Ensembl
Innerchr7:101812662..101900914hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3888250
hg1988250
hg1888253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607998
Supporting Variants
Samples
Known GenesALKBH4, LOC100630923, LRWD1, MIR4467, MIR5090, ORAI2, POLR2J, PRKRIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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