A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031868



Internal ID19121090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116066..189720hg38UCSC Ensembl
Innerchr7:116066..189720hg19UCSC Ensembl
Innerchr7:211149..284803hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3873655
hg1973655
hg1873655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654217
Samples
Known GenesLOC100507642
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031868
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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