A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6537n100



Internal ID22792624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101318135..101512775hg38UCSC Ensembl
chr7:100961416..101156056hg19UCSC Ensembl
chr7:100748136..100942776hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38194641
hg19194641
hg18194641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016122, nsv1020456, nsv1017544, nsv1019056, nsv1016531, nsv1017844, nsv1019282, nsv1023475, nsv1018135, nsv1021156, nsv1020544, nsv1033659, nsv1019142, nsv1018124, nsv1033270, nsv1024423, nsv1019318, nsv1032481, nsv1030025, nsv1030543, nsv1029050, nsv1026627, nsv1022652, nsv1018765, nsv1030624, nsv1026130, nsv1031841, nsv1018915, nsv1019605, nsv1024733, nsv1034896, nsv1026450, nsv1017707, nsv1032617, nsv1026144, nsv1034171, nsv1022477
Samples
Known GenesCOL26A1, RABL5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6537n100
Frequency
Sample Size11257
Observed Gain83
Observed Loss0
Observed Complex0
Frequencyn/a


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