A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584877



Internal ID20957948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30625643..31100945hg38UCSC Ensembl
chr17:28952661..29427963hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38475303
hg19475303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241777
Samples
Known GenesADAP2, ATAD5, CRLF3, DPRXP4, LRRC37BP1, MIR4733, NF1, RNF135, SH3GL1P2, SUZ12P1, TEFM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584877
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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