A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027091



Internal ID18769623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124671688..124748854hg38UCSC Ensembl
Innerchr7:124311742..124388908hg19UCSC Ensembl
Innerchr7:124098978..124176144hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3877167
hg1977167
hg1877167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662139
Samples
Known GenesGPR37
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027091
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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