A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615708



Internal ID20988779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77345101..77620000hg38UCSC Ensembl
chr7:76974418..77249317hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38274900
hg19274900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231362
Samples
Known GenesGSAP, PTPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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