A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6364n100



Internal ID22792451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56714602..56908389hg38UCSC Ensembl
chr7:56782295..56976080hg19UCSC Ensembl
chr7:56749789..56943574hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38193788
hg19193786
hg18193786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020183, nsv1027491, nsv1032918, nsv1021053, nsv1017473, nsv1017429, nsv1019506, nsv1033591, nsv1027775, nsv1021536
Samples
Known GenesLOC100130849
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6364n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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