A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615381



Internal ID6655580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146661210..146757069hg38UCSC Ensembl
chr7:146358302..146454161hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3895860
hg1995860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12997918
SamplesHG03814
Known GenesCNTNAP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615381
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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