A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017756



Internal ID19106973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13616511..13693981hg38UCSC Ensembl
Innerchr7:13656136..13733606hg19UCSC Ensembl
Innerchr7:13622661..13700131hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3877471
hg1977471
hg1877471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6282n100
Supporting Variantsnssv3643139
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)nsv1017756
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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