A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019992



Internal ID19109211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40404054..40440124hg38UCSC Ensembl
Innerchr7:40443653..40479723hg19UCSC Ensembl
Innerchr7:40410178..40446248hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3836071
hg1936071
hg1836071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6339n100
Supporting Variantsnssv3661213, nssv3661212
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)nsv1019992
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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