A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656828



Internal ID9922933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37460968..37462158hg38UCSC Ensembl
chr4:37462590..37463780hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6505616, essv6260590, essv5749671, essv5998136, essv5858340, essv6582722, essv5998012, essv6495458, essv5474645, essv5706235, essv6567009, essv6384735, essv6083312, essv6482916, essv5589788, essv5999180, essv6241959, essv6286093
SamplesNA19350, NA19920, NA19374, NA19373, NA19916, NA19917, NA19137, NA19471, NA19239, NA18867, NA18951, NA19461, NA18945, NA19390, NA19240, NA18501, NA19468, NA19463
Known GenesC4orf19
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656828
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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