A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978110



Internal ID12631967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21889458..22889658hg38UCSC Ensembl
Innerchr19:22072260..23072460hg19UCSC Ensembl
Innerchr19:21864100..22864300hg18UCSC Ensembl
Innerchr19:21864100..22864300hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381000201
hg191000201
hg181000201
hg171000201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34340
Supporting Variants
SamplesNA11839
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978110
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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