A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091876



Internal ID15945062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100776465..100899511hg38UCSC Ensembl
Innerchr7:100374087..100497131hg19UCSC Ensembl
Innerchr7:100212023..100335067hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38123047
hg19123045
hg18123045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607965
Supporting Variants
Samples
Known GenesACHE, EPHB4, MIR6875, SLC12A9, SRRT, TRIP6, UFSP1, ZAN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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