A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2797359



Internal ID21242697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30624837..30625592hg38UCSC Ensembl
chr17:28951855..28952610hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683865
Samples
Known GenesLRRC37BP1, SH3GL1P2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2797359
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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