A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9872595



Internal ID6497888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16911922..16940201hg38UCSC Ensembl
chr1:17238417..17266696hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3828280
hg1928280
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585353
Supporting Variants
SamplesNA21099
Known GenesCROCC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9872595
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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