A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091877



Internal ID15598377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100824534..100920838hg38UCSC Ensembl
Innerchr7:100422156..100518458hg19UCSC Ensembl
Innerchr7:100260092..100356394hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3896305
hg1996303
hg1896303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607966
Supporting Variants
Samples
Known GenesACHE, EPHB4, MIR6875, SLC12A9, SRRT, TRIP6, UFSP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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