A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026851



Internal ID19116069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27305180..27330932hg38UCSC Ensembl
Innerchr7:27344799..27370551hg19UCSC Ensembl
Innerchr7:27311324..27337076hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3825753
hg1925753
hg1825753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643325
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)nsv1026851
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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