A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024168



Internal ID19113385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10528064..10684870hg38UCSC Ensembl
Innerchr7:10567691..10724497hg19UCSC Ensembl
Innerchr7:10534216..10691022hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38156807
hg19156807
hg18156807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642913
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024168
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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