A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203502



Internal ID20770542
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 StatusS
Merged Variantsnsv6316887
Supporting Variants
Samples
Known GenesGPR3, WASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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