A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535511



Internal ID20908872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61914428..61915067hg38UCSC Ensembl
chr17:59991789..59992428hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037133
Samples
Known GenesINTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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