A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981745



Internal ID12625933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22482546..24321183hg38UCSC Ensembl
Innerchr19:22665348..24503985hg19UCSC Ensembl
Innerchr19:22457188..24295825hg18UCSC Ensembl
Innerchr19:22457188..24295825hg17UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg381838638
hg191838638
hg181838638
hg171838638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751784
Supporting Variants
SamplesBEC_333
Known GenesHAVCR1P1, LOC100132815, LOC100996349, LOC440518, RPSAP58, ZNF254, ZNF492, ZNF675, ZNF681, ZNF724P, ZNF726, ZNF728, ZNF730, ZNF91, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981745
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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