A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979441



Internal ID12633498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75594419..75679819hg38UCSC Ensembl
Innerchr2:75821545..75906945hg19UCSC Ensembl
Innerchr2:75675053..75760453hg18UCSC Ensembl
Innerchr2:75733200..75818600hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3885401
hg1985401
hg1885401
hg1785401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34608
Supporting Variants
SamplesNA18555
Known GenesGCFC2, MRPL19
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979441
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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