A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316887



Internal ID20849969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27394088..27413080hg38UCSC Ensembl
chr1:27720592..27739574hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3818993
hg1918983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203502
Samples
Known GenesGPR3, WASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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