A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321340



Internal ID20854444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37520461..37538261hg38UCSC Ensembl
chr1:37986062..38003862hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3817801
hg1917801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202458
Samples
Known GenesSNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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