A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6458n100



Internal ID22792545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72350322..72393182hg38UCSC Ensembl
chr7:71815307..71858167hg19UCSC Ensembl
chr7:71453243..71496103hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3842861
hg1942861
hg1842861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019885, nsv1023385
Samples
Known GenesCALN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6458n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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