A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6348n100



Internal ID22792435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51527881..51569575hg38UCSC Ensembl
chr7:51595578..51637272hg19UCSC Ensembl
chr7:51563072..51604766hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3841695
hg1941695
hg1841695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015652, nsv1018638
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6348n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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