A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027075



Internal ID19116294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40398879..40440124hg38UCSC Ensembl
Innerchr7:40438478..40479723hg19UCSC Ensembl
Innerchr7:40405003..40446248hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3841246
hg1941246
hg1841246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6339n100
Supporting Variantsnssv3643880
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027075
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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