A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512072



Internal ID20885402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30625320..30823631hg38UCSC Ensembl
chr17:28952338..29150649hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38198312
hg19198312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194239
Samples
Known GenesCRLF3, LRRC37BP1, SH3GL1P2, SUZ12P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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