A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607999



Internal ID16048722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102451288..102473452hg38UCSC Ensembl
Innerchr7:102091735..102113899hg19UCSC Ensembl
Innerchr7:101878740..101900904hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3822165
hg1922165
hg1822165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091993
Samples
Known GenesALKBH4, LRWD1, MIR4467, MIR5090, ORAI2, POLR2J
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607999
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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