A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018400



Internal ID19107617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13156663..13268849hg38UCSC Ensembl
Innerchr7:13196288..13308474hg19UCSC Ensembl
Innerchr7:13162813..13274999hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38112187
hg19112187
hg18112187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643125
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)nsv1018400
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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