A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6368n100



Internal ID20157984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56997641..57607573hg38UCSC Ensembl
chr7:57065348..57667279hg19UCSC Ensembl
chr7:57069290..57671221hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38609933
hg19601932
hg18601932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031756, nsv1032599, nsv1019165
Samples
Known GenesGUSBP10, MIR3147, ZNF479, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6368n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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