A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615384



Internal ID6655583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146761026..146798964hg38UCSC Ensembl
chr7:146458118..146496056hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3837939
hg1937939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12998047
SamplesHG03814
Known GenesCNTNAP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615384
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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