A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646829



Internal ID7033572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30431384..30451651hg38UCSC Ensembl
chr21:31803702..31823969hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3820268
hg1920268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv810e214
Supporting Variantsessv16310568, essv16310569, essv16310567
SamplesNA19026, NA19455, NA18873
Known GenesKRTAP15-1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646829
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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